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Abdomen, Digestive system surgery, Surgical removal procedures, Surgical procedures and techniques, Surgery
Abdomen, Digestive system surgery, Surgical removal procedures, Surgical procedures and techniques, Surgery
Latest novoGI News
May 4, 2022
Hand-Sewn Anastomosis Hand-suturing represents the classical anastomosis method and is primarily used in open surgery. Absorbable or non absorbable suture materials can be used. 4 , 6 , 16 , 17 Generally, the design of the hand seam is determined by the number of rows, the layering, the suturing technique and the adaptation technique. 6 , 18 , 19 There is a lack of significant research (prospective/randomized trials) comparing and evaluating the surgical outcomes of the various hand-suturing parameters, so no clear superiority of one of the diverse influencing variables could be determined so far. 20 Some groups established that there is no significant difference between single-layer or double-layer techniques concerning postoperative complications. 21–23 Others detected lower postoperative complication rates for continuous than for interrupted suture anastomoses 24 or concluded the superiority of inverted anastomoses compared to everted anastomoses. 22 , 25 However, these studies only have restricted significance due to their limited scope size and study design. For simplification, and due to the absence of significant advantages, all hand suturing techniques were summarized as one. Stapling Anastomosis With the beginning of laparoscopy in the 1990s, stapling systems became increasingly important and quickly developed into the most commonly used anastomosis technique. 6 , 26 , 27 Releasing the applicator, the staples are inserted permanently into the tissue and thus connect the two segments after intestinal resection. 26 Depending on the shape of the system, various principles of stapling devices can be distinguished. These include linear staplers, which are available for both open surgery and laparoscopic procedures, as well as transverse, and circular staplers. 6 Furthermore, 2- and 3-row systems can be distinguished, and pure stapling devices can be separated from stapler/knife combinations in so-called GIAs (derived from Gastrointestinal Anastomosis). 26 Using linear, multi-row staplers, the intestine can be cut by the integrated knife while closing the lumina linearly at multiple points simultaneously. In this way, two intestinal segments are obtained closed at the ends. 26 Circular staplers consist of a main body with a staple cartridge and a removable counter-pressure plate, by which means two tissue parts can be connected in the form of an inverting or everting anastomosis. 26 The adaption to various intestinal lumen diameters is enabled by a selection of systems in various diameters (21–34 mm) 26 or lengths (30–90mm). Staplers in general feature a rigid body and vary according to their diameter and length, and whether they can be used in open or laparoscopic surgery. The Surg-ASSIST computer-assisted stapling system from Power Medical Interventions (New Hope, PA, USA) has been available since 2004. This system is comprised of a flexible, autoclavable shaft to which various types of stapling magazines (eg, linear or circular) can be connected, a computer, and a remote control device. The increased flexibility of the shaft and the instruments was intended to improve accessibility of the resection site in anatomically difficult regions. The computer-control device provided contact pressure assessment on the tissue before triggering and was supposed to enable automatic adaptation to the tissue quality. 28 Although the system disappeared from clinical usage, some interesting specifications of this system were at least partially realized in other products currently available on the market. An example of this are motor-driven stapling systems (eg, Medtronic/Johnson & Johnson), allowing for high precision and maneuverability for adoption to various tissue and patient conditions (Covidien Medtronic). Compression Anastomosis This technique uses two-piece compression implants that are inserted into the intestinal lumina and then connected to compress the tissue between the two implant segments. 4 The permanent compression causes the tissue to grow together and consequently leads to a permanent connection. 4 Most of the available systems are automatically expelled due to compression-related tissue necrosis 4 , 29 , 30 leaving a foreign body free anastomosis in the organism. In some products, this is supported by additional biodegrading mechanisms. 29 , 30 An early example of compression anastomosis implants was “Murphy’s Button”, 31 which vanished from the scene due to unsatisfying clinical outcomes. 4 , 30 Recent compression anastomosis systems can be distinguished by their implant halves’ interlocking mechanism and the principle of permanent pressure application into form fit, shape memory, and magnet-based implants. While the compression rings in form fit-based systems (eg, AKA-2 (Seidel, Medipool, Friedrichsthal, Germany), 4 , 29 , 30 , 32 Valtrac, “Biofragmentable Anastomotic Ring” (BAR) (Sherwood-Davis & Geck, St. Louis, MO, USA) 4 , 6 , 12 , 30 , 33 , 34 and RapAn 4 , 35 ) consist of dimensionally stable materials (Metal, Polyetherketone or Polyglycolic acid), shape memory-based implants use the temperature-dependent shape changing effect of Nickel Titanium Alloy (NITINOL) for pressure application (eg, “Compression Anastomosis Clip” (CAC) (NiTi Alloys Technologies, Ltd., Netanya, Israel), “Compression Anastomosis Ring” (NiTi CAR or ColonRing) (novoGI Inc. formerly NiTi Surgical Solutions Ltd., Netanya, Israel)). 30 , 36–40 Both principles require mechanical closure mechanisms for the connection of the ring elements. This is in contrast to magnet-based compression anastomosis, in which the attraction forces between the polarized implant halves enable an anastomosis closure. Due to the simplicity of the underlying principle, available systems do not require complex application devices and are the only systems suitable for endoscopic use (Magnamosis implant (Harrison Rings) (Magnamosis Inc., San Francisco, CA, USA), 41–46 “Smart self-assembling Magnets for Endoscopy”- system (SAMSEN)/“Incisionless Magnetic Anastomosis System” (IMAS) (both GI Windows Inc., West Bridgewater, MA, USA)). 47–50 In compression anastomosis, all evaluated principles were also summarized in one group, since no comparative studies or evidence of superiority of any of these systems is reported by the literature. Clinical Evaluation of Current Anastomosis Techniques Comparison of Hand-Sewn and Stapled Anastomosis Since minimized complication risk is the most fundamental aspect when reconnecting two residual lumen segments, postoperative outcomes of reported clinical in-human trials are described and analyzed in detail in the following section. Table 1 lists studies on clinical results of hand-suture and stapler anastomoses. Table 1 Hand-Sewn and Stapler Anastomoses: Clinical Results The summative effect for any adverse event is further analyzed by assessing the respective odds ratio as indicated in Figures 2 and 3 and comprehensively outlined in Table 1 . Figure 2 Meta-analysis: Risk of anastomotic leak for comparison of stapler (experimental) and hand-sewn (control) anastomosis. Figure 3 Meta-analysis: Risk of anastomotic stenosis for comparison of stapler (experimental) and hand-sewn (control) anastomosis. Analyzing the incidence rates of postoperative complications, including bleeding, wound infections, abscesses, anastomotic hemorrhages, pulmonary embolisms, and fistulas, McGinn et al revealed a clear superiority of the hand suture technique with a complication rate double as high for the stapled anastomosis. 61 In comparison, Cheregi et al show a reverse trend, revealing incidence rates twice as high for the hand-suture anastomoses than for the stapler anastomoses. 54 However, the majority of the meta-analyses and clinical trials 51 , 56 , 60 , 64–66 as well as our assessment ( Table 1 ) show that both techniques cause similarly high incidence rates for these kinds of complications. For the most critical postoperative complication, anastomotic leakage, early studies such as the one of McGinn et al showed significantly higher leakage rates for stapler than for hand-suture anastomoses. 61 However, more recent and powerful studies and meta-analyses based on larger patient scopes, such as those of Adloff et al, Everett et al, Neutzling et al, and Polese et al revealed a similar trend and nearly equal leakage incidence rates for both techniques. 10 , 51 , 57 , 66 This outcome is confirmed by our meta-analysis ( Figure 2 ). Concerning the need for reoperation, different conclusions can be found in literature. Whilst Everett et al revealed results in favor of the hand-suture anastomosis, Adloff et al determined lower reoperation rates for the stapler technique. 51 , 57 However, available meta-analyses, such as from He et al and Neutzling et al, show that a clear superiority of one technique over the other cannot be deduced for this aspect, 66 , 67 and our assessment also showed no significant differences ( Table 1 ). Concerning the risk of stenosis, our assessment and meta-analysis identified a significant superiority of the hand-sewn technique when compared to staples ( Figure 3 ). This effect is mainly contributed by the study of Polese et al, who specifically investigated the effect of stapling techniques on the occurrences of obstructions and deduced that stapling anastomoses favor the development of stenoses. 10 These findings differ from available meta-analyses that showed similar results for the obstruction rate. 64–66 , 68 Finally, the intervention-related mortality rate was calculated for the respective subgroups by most authors, 51–56 , 59–61 , 63 and here no significant differences were observed. Accordingly, our meta-analysis also did not reveal any significant effect on this event ( Table 1 ). In summary, most authors concluded that stapling is at least as safe to use as hand-sutured anastomosis . Positive features of stapling anastomosis devices include their applicability in narrow regions (eg, for anterior rectal resection) 51 and the reduction in surgery time. 69 , 70 However, studies also report technical complications that have arisen with the stapling method, such as Everett et al, who reported technical complications in 6 of the originally planned 50 patients in the stapler group (rate of incomplete tissue doughnuts: 13.6%). The risk of stenosis, however, seems to be increased with mechanical anastomoses, but mainly due to the results of one single study. Comparison of Compression Type and Conventional (Hand-Sewn/Stapled) Anastomosis For compression anastomoses, only a few (comparative) studies, which are outlined in Table 2 , have been published on this technique so far. It is important to mention that the volume of included patients is comparably low and the according risk of bias is therefore higher in these trials. For the most recent principles (mainly magnet-based compression anastomosis), not a single comparative study is available to date. Nevertheless, and to identify potential advantages of these techniques, some relevant (non-comparative) studies are supplemented with Table 3 but are handled self-contained. Table 2 Compression Anastomosis Systems: Clinical Results Table 3 RapAn, The AKA-2, Magnamosis, and IMAS – Postoperative Outcomes of Preliminary Clinical Studies Unfortunately, no comparative studies on the various techniques for compression anastomoses are published to date; we therefore had to consider all available techniques for meta-analyses as one. However, we did perform a selective assessment of the comparison of compression techniques to staples and hand-sutures, respectively. Additionally, since form fit and shape memory-based compression anastomosis systems might offer different results and are also investigated separately in literature, we will selectively outline the respective results for each of these techniques. Overall Assessment of Compression Type Anastomosis in Comparison to Hand-Sewn and Stapled Principles As shown by meta-analysis and Figures 4 – 7 , as well as in Table 2 , no statistically significant differences were observed for the respective techniques in terms of postoperative leaks, surgical site infections, the need for reoperations, or mortality rates. Of note, and in contrast to some comparative studies that highlight the superiority of compression-type anastomoses in terms of risk of stenoses, no advantages were observed for this parameter, neither in comparison to the hand suturing ( Figure 7 ) nor in comparison to stapled anastomoses ( Figure 5 ). Figure 4 Meta-analysis: Risk of anastomotic leak for comparison of compression (experimental) versus stapler (control) type anastomosis. Figure 5 Meta-analysis: Risk of anastomotic stenosis for comparison of compression (experimental) versus stapler (control) type anastomosis. Figure 6 Meta-analysis: Risk of anastomotic leak for comparison of compression (experimental) versus suture (control) type anastomosis. Figure 7 Meta-analysis: Risk of anastomotic stenosis for comparison of compression (experimental) versus suture (control) type anastomosis. Form fit-Based Compression Anastomosis Only comparative studies evaluating technique associated postoperative complication rates for the Valtrac BAR device have been conducted until recently. Due to the limited number of patients, no conclusive statements can be drawn about the eligibility and safety of the systems. For example, Galizia and Pahlman et al detected a slightly higher leakage rate for the BAR than for conventional techniques, 74 , 80 whilst Cahill, Bubrick, Gullichsen, and Chen observed an inverse tendency. 71–73 , 75 The reoperation rate was only evaluated by the studies of Gullichsen, Galizia, Pahlman, and Chen et al, 73–75 , 80 whilst Chen observed a higher reoperation rate for the BAR than for hand-suture anastomoses, 73 Gullichsen, Galizia, and Pahlman established results in favor of the BAR. 74 , 75 , 80 Except for Chen et al, all other authors derived lower mortality rates for the BAR than for the other techniques. 71–73 , 75 , 80 The majority of clinical trials (Cahill, Bubrick, Gullichsen, Seow-Choen, and Galizia et al) observed that postoperative complications such as bleeding, wound infections, abscesses, anastomotic hemorrhages, pulmonary embolisms, and fistulas occurred more often in compression anastomoses than in hand or stapler anastomoses. 71 , 72 , 74 , 75 , 81 Based on the available results, the BAR allows just as safe clinical use as conventional techniques. 71–75 Gullichsen et al detected no significant difference between the groups in the recovery of the gastrointestinal tract. 75 Concerning additional features, the fast application of the BAR was highlighted as a particular advantage even in direct comparison to stapling anastomoses. 72 , 74 , 83 In the study of Cahill et al, technical problems occurred in 11.9% of the cases in the BAR group. In four of these, the BAR could not be used due to dimensional restrictions and had to be replaced by another technique. 72 Shape Memory-Based Anastomosis Systems In the area of nitinol-based compression anastomoses, two systems can be distinguished, namely the ColonRing, also known as CAR, and the CAC. The compression anastomosis clip was only investigated by the group of Nudelman et al. This study shows at least equal results (leakage and mortality rates) or even slight advantages (obstruction, reoperation, and wound infection/bleeding/abscess rates) in favor of the CAC. 79 According to the author, these slight advantages could derive from the less traumatic insertion techniques and the expulsion of the compression implants after healing. 79 However, the patient population of 60 persons is too small to derive reliable statements about this system. More evidence is available on the CAR, which shows similar results compared to the conventional stapler technique in all evaluation dimensions, 76 , 77 , 82 in particular with regard to the anastomosis leakage rate. The respective authors summarized concordantly that the CAR can be used as safely and effectively as staplers in colonic anastomosis surgeries. 76 , 77 , 82 , 84 , 85 Moreover, Koo et al detected a slight superiority of the CAR regarding a reduced occurrence of stenoses, since they observed wider and more patent anastomoses for the CAR in a 6-month follow-up colonoscopy, in contrast to narrowed stapler anastomoses (due to the foreign body reactions caused by the staples permanently remaining within the body). 76 Another reason for the reduced stenosis rate of the CAR mentioned in literature might be the larger anastomosis lumen as a result of implant excretion after necrosis. 86 Tulchinsky et al observed no statistically significant differences in postoperative courses, recoveries, or hospital stays between CAR and stapler groups. 76 , 82 Koo et al stated that the operation duration was also comparable for both techniques. 76 Separate Considerations on New Compression Principles RapAn, The AKA-2, Magnamosis, and IMAS For these systems, neither major clinical studies, nor meta-analyses, nor systematic reviews have been performed so far. For the sake of completeness, 4 clinical, but not comparative human trials were selectively chosen to represent preliminary clinical results of the four missing RapAn, the AKA-2, Magnamosis, and IMAS systems. Since these studies do not meet the inclusion criteria of our methods and the patient population is far too small to draw representative conclusions, they are not included in the detailed anastomoses technique performance evaluation. Summary of Meta-Analysis Results All methods and implant types were analyzed and compared with respect to their risk of postoperative complications. There was no statistically significant difference in the occurrence rate for bleeding, wound infections, abscesses, anastomotic hemorrhages, pulmonary embolisms, fistulas, revision indications, mortality, or anastomotic leakages between hand-suture and stapling techniques. Concerning the risk of stenosis, our assessment and meta-analysis identified a significant superiority of the hand-sewn technique compared to staples. The overall assessment of compression-type anastomosis in comparison to hand-sewn and stapled principles showed that there was no significant difference in terms of postoperative leaks, surgical site infections, needs for reoperation, mortality rates, nor for the risk of stenoses, either between compression and hand suture or in comparison to stapled anastomoses. Discussion Are We Already Completely Satisfied with the Available Techniques? Perfect anastomosis healing is essential for the successful recovery process of patients. 8 Anastomotic insufficiencies following resective surgery in the gastrointestinal tract are among major risks for serious complications such as peritonitis, sepsis, or complication-related deaths. 8 , 9 , 15 An important prerequisite for the ideal anastomosis is a stress-free contact of wound edges, which ensures sufficient blood supply. 8 , 26 In this respect and aside from physiological aspects, the method of how the anastomosis is created deserves particular attention. One might expect that as surgical methods evolved and new technologies became available, anastomosis-related complications would have been reduced to almost zero. However, and despite a variety of implants and methods and irrespective of any technical and instrumental progress, current studies still show relatively high complication risks, such as anastomosis leakage rates of up to 10% and stenoses. Complications related to anastomoses are leading causes for morbidity and mortality in visceral surgery and range among the main reasons to keep patients in the hospital for observation even after a successful intervention. Accordingly, we need to question available methods. In the age of digitalization and robotics, new tools will have an increasing effect on surgery and patient treatment standards in the future. In this context, a detailed investigation of available techniques can reveal potentials that may contribute to the invention of new devices allowing for minimally invasive interventions. Thus, we assessed the techniques’ current performances and further potentials for surgical trauma reduction, comprising the susceptibility to postoperative complications such as leakages or obstructions. Further considered aspects were the simplicity and standardization of the procedure (independence of the interventional outcome or the surgeon’s level of experience), a foreign body poor or even free anastomosis site, as well as the techniques’ and devices’ applicability in regions with a lack of manipulation space as a measure for usability via minimal (amount and size) incisions. All of these are aspects that have already paved the way for mechanical anastomosis. 11 To provide a general assessment of available techniques, we compared all principles in our meta-analysis where no statistically significant difference between either of the techniques was established except for an increased risk of stenoses for stapler compared to hand suture anastomoses, and we discussed the methods with respect to the aforementioned aspects. According to these criteria, all techniques, first and foremost the hand-suture anastomosis, showed significant shortcomings. One of the biggest problems, with respect to current trends and future needs, is its low standardization potential and the need for extensive access to reach the organ and allow manipulation, hampering minimization of incisions. But are stapling anastomoses really the better option? Staplers indeed allow for an anastomosis formation that is less dependent on the surgeons´ individual skills and safe operating times. When compared to hand-suture anastomoses, staplers show an increased risk for stenoses, an assumption that has also been deduced by others. 7 , 10 , 65 Polese et al specifically identified the staple-suture as one of the most critical risk factors for anastomosis stenoses in their study. 10 It will thus become interesting to observe whether newer systems using an additional stapling row will lead to even more stenoses. Furthermore, staplers are not the perfect solution in other aspects, since various research groups have identified an increased risk of anastomosis leakages associated with an increasing number of stapler releases 87–90 and increasing stapler device diameters. 89 One of the major problems with stapling systems, limiting their suitability for minimized or even natural access routes, are the high forces required to enable plastic deformation of staple seams. 91 One approach to overcome this problem is the trend to digitalization and mechatronification. Whereas this trend had already started years before with the computer-assisted, flexible stapler system by Power Medical Interventions Deutschland GmbH, it has recently been reintroduced. While the first system showed some significant weaknesses, for example, failure of the entire mechatronics system in 3% of patients, 92 new powered stapling systems, such as Signia Stapling System (Medtronic GmbH, Germany) (Covidien Medtronic) and ECHELON CIRCULAR Powered Stapler (Ethicon Inc. by Johnson & Johnson Medical N.V., Belgium) (Johnson & Johnson) have increasingly established themselves in clinical practice. More recent evaluations demonstrated that they enable easier intraoperative handling and reduced malformation of staples. 93 , 94 However, these systems still have rigid bodies required to apply the significant forces at the device tip. Therefore, this technology is limited to the transabdominal application excluding anastomoses in the lower sigma or rectum. Endoluminal stapling anastomosis in higher parts of the colon, which requires endoscopic device solutions, is not feasible so far due to a lack of force transmission methods along flexible endoscope shafts. The development of force-efficient closure mechanisms of compression anastomosis implants could potentially bring about a significant step towards innovative procedures. Furthermore, these systems show a comparable potential for standardization and independence of the surgeon’s level of experience as staplers, which is advantageous compared to hand suturing and would potentially allow minimization of access routes. Furthermore, it has been shown that compression anastomoses can potentially be compared with conventional and staple suturing techniques in terms of safety and surgical outcome, or in some cases even produce better results. 32 , 35 , 36 , 38 , 77 , 86 , 95 , 96 Especially, the expulsion of the compression implants enabling a foreign-body-free healing process, leading to less scarring, deserves notice. In their meta-analysis, however, Slesser et al concluded that there were no advantages with regard to postoperative complications in favor of compression anastomoses 15 and our meta-analysis also did not provide any evidence of superiority. In addition, it must be considered that the number of included patients in available studies is low and thus the available evidence is limited, which is why further studies are required to assess outcomes of compression anastomoses more thoroughly. Additionally, in terms of system design, most available devices still suffer from significant weaknesses when it comes to the goal of avoiding artificial incisions from the outside and reducing surgical trauma during placement procedures. During incisionless, endoscopic applications, anastomotic implants must cover a certain system size variance since dimensional demands vary during the insertion process via natural orifices. During insertion and navigation to the anastomosis site, the system must be as small as possible to minimize the diameter increase of the inserted endoscopes and to avoid restriction of shaft flexibility. To manipulate and reconnect the two free lumina after the resection, however, the system must adjust to the bowel walls, underlying certain variations due to patients’ individual colon diameters. For subsequent implant excretion, the system must again be small enough to pass through natural human orifices. IMAS is the only implant addressing these requirements. It is currently in the FDA approval phase and further investigative studies must be conducted to distinctively assess its performance in comparison to conventional techniques. Limitations of Our Study This study is in first line limited by the heterogeneity of available studies and the different representation of available methods in literature. Especially compression anastomoses, potentially seem rather underrepresented because some principles have not yet been introduced, and were only investigated in small studies. The latest studies no longer include hand-sewn techniques; thus, a comparison of new principles to established standards is missing. For compression anastomosis, no comparison of the various available techniques (form fit versus memory shape versus magnet-based) was performed until recently, so no reliable assessment of either method seems possible. Accordingly, larger randomized controlled trials are needed that should involve the principles addressed herein. Summary and Conclusion Considering the results of the clinical studies analyzed, some of which still tend to show high postoperative complication rates, it must be concluded that the anastomosis systems currently available in gastrointestinal surgery still leave room for improvement. In the age of digitalization and robotics, technology and the invention of new tools will have an increasing effect on surgery and treatment standards of the future. In this context, a detailed investigation of available techniques can reveal potentials that may contribute to the invention of new devices allowing for minimally invasive interventions. The available studies do not show a clear superiority of any one type of anastomosis, which is why it is concluded that the dominance of the currently prevalent stapler anastomoses should at least be questioned. Even if compression anastomoses still occupy a niche position, we assume that the development opportunities of implant-based anastomosis formation, such as the force-effective tissue reconnection and high standardization, should be taken seriously and considered for future projects and innovative devices, to meet the demands of modern visceral surgery in the future. Registration, Review Protocol. and Accessibility of Data The review was not registered, and no review protocol was prepared. Data used for this review are publicly available. Ethical Approval This article does not contain any studies containing animals or human participants performed by any of the authors. Author Contributions All authors contributed to data analysis, drafting, or revision of the article have agreed on the journal to which the article will be submitted, have given final approval of the version to be published, and agree to be accountable for all aspects of the work. Funding Disclosure Prof. Wilhelm, Prof. Mela, Dr. Eblenkamp, Dr. Jell, Mr. Ostler, Ms. Ficht and Ms. Steger report grants from DFG, German Research Foundation, during the conduct of the study. In addition, Prof. Wilhelm, Prof. Mela, Dr. Eblenkamp, Mr. Ostler, Ms. Ficht and Ms. Steger have two patents pending; 1) Clamping device and applicator for joining flexible tubular walls (International publication number: WO 2022/049196 A1) and 2) Implant and implant applicator for surgical anastomosis (International publication number: WO2022/049197 A1). The authors report no other conflicts of interest in this work. References 1. Chawla N, Butler EN, Lund J, Warren JL, Harlan LC, Robin YK. Patterns of colorectal cancer care in Europe, Australia, and New Zealand. J Natl Cancer Inst Monogr. 2013;2013(46):36–61. doi:10.1093/jncimonographs/lgt009 2. Covidien Medtronic: covidien Medtronic signia stapling system. Online verfügbar unter: https://www.medtronic.com/covidien/en-us/products/surgical-stapling/signia-stapling-system.html . Accessed
novoGI Frequently Asked Questions (FAQ)
When was novoGI founded?
novoGI was founded in 1996.
Where is novoGI's headquarters?
novoGI's headquarters is located at Netanya.
What is novoGI's latest funding round?
novoGI's latest funding round is Dead.
How much did novoGI raise?
novoGI raised a total of $18.5M.
Who are the investors of novoGI?
Investors of novoGI include Forbion Capital Partners, Meakem Becker Venture Capital, Israel Healthcare Ventures, Alice Ventures, SCP Vitalife and 3 more.
Who are novoGI's competitors?
Competitors of novoGI include BioProtect, Expanding Orthopedics, nContact Surgical, ConforMIS, BeneChill and 10 more.
Compare novoGI to Competitors
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Axial Biotech, founded in 2002 by a group of spine surgeons and geneticists, is focused on the use of genetics and the development of minimally invasive fusionless devices to advance the diagnosis and treatment of diseases and deformities of the human spine. Axial is a company to pursue DNA-based pre-symptomatic and prognostic tests for common spinal conditions which will augment current clinical and surgical practices. In its initial genetic product development initiative, Axial has made progress towards the discovery of a location in the human genome that is associated with adolescent idiopathic scoliosis. In addition, Axial's founders have developed five motion preserving, fusionless surgical devices (including such device currently being implanted in humans) that have the promise of expanding the current treatable scoliosis patient population by a factor of ten. Axial intends to use its genetic intellectual property in the development of bio-mechanical devices, and to apply its gene discovery/product development methodology to other spinal diseases. Axial (www.axialbiotech.com) is located in Salt Lake City, Utah.
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Axis Surgical Technologies, Inc. aims to develop, manufacture, and market devices that improve quality and efficiency in spinal surgery, especially for minimally invasive surgical techniques. Based in Mountain View, California, Axis offers an integration of visualization and articulation capabilities and provides spinal surgery equipment.Axis' FDA Grant In March 2010, Axis announced that it received 510(k) clearance from the Food and Drug Administration to market its C-MOR„ Visualization Device to use in diagnostic and operative arthroscopic and endoscopic procedures. This portable tool provides visualization and illumination of an interior cavity through either a natural or surgical opening. The ergonomic lightweight device also offers practitioners the convenience of endoscopic visualization and efficient one-handed operating ability; this device can be employed in hospital outpatient departments, ambulatory surgery centers, and office surgery suites.
NeoChord is a medical technology company engaged in the advancement of beating heart mitral valve repair in patients suffering from mitral valve regurgitation. The company's flagship product, the NeoChord Artificial Chordae Delivery System, is a beating heart procedure, echo-guided treatment for patients with mitral valve regurgitation and is proven to resolve and restore normal mitral valve function. The company was founded in 2007 and is based in Minneapolis, Minnesota.
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