Somnus Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 16
What Somnus Medical Technologies, Inc. makes
The company manufactures electrosurgical generators, including models like the S1, 215, 225, 615, and S2, designed for tissue coagulation and cutting procedures. It also produces disposable and reusable electrodes, such as the tissue coagulating electrode, multiple electrode coagulating probe (Model 350), and bendable electrodes with bending tools. Additionally, the company supplies the Somnoplasty System, a device used for tissue coagulation in medical procedures.
The portfolio consists of Class II devices, all of which are listed via the FDA’s 510(k) pathway. These products are regulated under U.S. medical device laws and appear in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 16 devicesFrequently asked questions
How many devices does Somnus Medical Technologies, Inc. have in the registry?
The registry currently lists 16 devices for Somnus Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Somnus Medical Technologies, Inc.'s devices?
Among its 16 most recently registered devices, Somnus Medical Technologies, Inc. has devices listed in FDA 510(k) (16 devices).
What risk classes do Somnus Medical Technologies, Inc.'s devices fall under?
Among its 16 most recently registered devices, the classes recorded for Somnus Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Somnus Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Somnus Medical Technologies, Inc. include ELECTROSURGICAL GENERATOR, MODEL S1, SOMNUS MODEL 225 ELECTRO SURGICAL GENERATOR (MODEL 225), SOMNUS MODEL 615 ELECTROSURGICAL GENERATOR(MODEL 615) and SOMNOPLASTY SYSTEM.