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Founded Year

2000

Stage

Series E | Dead

Total Raised

$79.65M

Last Raised

$25.3M

About Satiety

Satiety, Inc. is a medical device company focused on the development of less invasive devices for the treatment of obesity. Obesity is a global health problem, affecting 70 million people in the U.S. and 300 million worldwide, and growth of which is causing increases in obesity-related diseases such as diabetes, high blood pressure and cardiovascular disease. Obesity surgery has been shown to be the only long-term effective means of weight loss for morbidly obese patients. Satiety's first product, the TOGA System, enables physicians to perform a procedure similar to traditional restrictive obesity surgeries, but without surgical incisions. In this procedure, the TOGA System devices are inserted transorally (through the mouth) and are used to reduce the capacity of the stomach to give patients a feeling of fullness after a small meal. The procedure is intended to be safer and easier for patients to tolerate than conventional obesity surgery. Safety and effectiveness of the TOGA System are currently being evaluated in a multi-center U.S. Study and the system is not available for sale in the United States.

Headquarters Location

2470 Embarcadero Way

Palo Alto, California, 94303,

United States

650-320-2100

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Satiety Patents

Satiety has filed 11 patents.

patents chart

Application Date

Grant Date

Title

Related Topics

Status

12/29/2006

5/28/2013

Digestive system surgery, Gastrointestinal tract disorders, Digestive system procedures, Medical equipment, Digestive system

Grant

Application Date

12/29/2006

Grant Date

5/28/2013

Title

Related Topics

Digestive system surgery, Gastrointestinal tract disorders, Digestive system procedures, Medical equipment, Digestive system

Status

Grant

Latest Satiety News

Comparison of Low GI and High GI Potatoes in Relation to Satiety (POSAT)

Nov 10, 2020

Comparison of Low GI and High GI Potatoes in Relation to Satiety (POSAT) Brief The study is a single-blind, randomised crossover study, investigating how a high glycaemic potato affects satiety in humans compared to a low glycaemic potato. This is done to shed further light on the discussion about whether potatoes with a high glycaemic index increases the risk of overweight and obesity and thus indirectly type 2 diabetes and cardiovascular disease. Detailed The POSAT study follows a single-blinded randomized crossover design. Each subject will have two separate intervention days with at least a six-day washout period in between. On the two intervention days the subjects will be randomized into receiving a breakfast containing isocaloric amounts of either low or high GI potatoes. VAS will be measured 5 minutes before the meal, immediately after the meal is consumed and in intervals of 30 minutes thereafter until 2,5 hours after the initial meal. After this the subjects will be served a standardized homogenous ad libitum meal. The amount of food consumed will be registered. The subjects will be asked to fast for 8-10 hours prior to the trial days and abstain from vigorous physical activity and alcohol consumption for 2 days prior to each trial day. The trial will be conducted over a total of 8 days with 5-6 study subjects pr. trial day. The trial days will be spread out over a total of 2 weeks to allow for a 1-week washout period between trial days for each subject. Eligibility Exclusion Criteria: Use of daily prescription medicine (mild analgesics and antihistamines are allowed). Use of medicine or dietary supplements that can affect ones appetite one month before the start of the study. Smoking or have been smoking or using any nicotine products (gum or e-cigarette) within the last 3 months. Irregular smoking is allowed. Elite athletes defined as doing >10 hours of strenuous physical activity per week. Participation in other clinical studies <1 month before or during the study. Inability, physically or psychologically, to comply with the procedures required by the study protocol. Judged by the investigators. Any food allergies. Inability to complete the trial within 3 months after screening. Unable to fast 8-10 hours before the trial days. Healthy Volunteers: Accepts Healthy Volunteers Gender: Male

Satiety Frequently Asked Questions (FAQ)

  • When was Satiety founded?

    Satiety was founded in 2000.

  • Where is Satiety's headquarters?

    Satiety's headquarters is located at 2470 Embarcadero Way, Palo Alto.

  • What is Satiety's latest funding round?

    Satiety's latest funding round is Series E.

  • How much did Satiety raise?

    Satiety raised a total of $79.65M.

  • Who are the investors of Satiety?

    Investors of Satiety include Venrock, Three Arch Partners, Morgenthaler Ventures, Pinnacle Ventures, HLM Venture Partners and 7 more.

  • Who are Satiety's competitors?

    Competitors of Satiety include NuVasive, NeoChord, Vertos Medical, EndoGastric Solutions, Epitomee Medical and 7 more.

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