Fountain Pharmaceuticals, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Fountain Pharmaceuticals, Inc. makes
Fountain Pharmaceuticals, Inc. manufactures SORBEX™ SOFT SPONGE, a disposable sponge designed for wound care and fluid absorption, and REDI-RELEASE ABSORBENT DRESSING, a dressing intended for managing exudate in wounds. Both products are intended for single-use applications in medical settings.
The company’s portfolio consists of Class I medical devices, regulated under the FDA’s 510(k) clearance pathway. These products are listed in the U.S. regulatory system and are based in the United States.
Catalogue
Sorbex(Tm) Soft Sponge Ref K895654
510(k) 510(k)Redi-Release Absorbent Dressing Ref K904604
510(k) 510(k)
Frequently asked questions
How many devices does Fountain Pharmaceuticals, Inc. have in the registry?
The registry currently lists 2 devices for Fountain Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fountain Pharmaceuticals, Inc.'s devices?
Among its 2 most recently registered devices, Fountain Pharmaceuticals, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fountain Pharmaceuticals, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fountain Pharmaceuticals, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fountain Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Fountain Pharmaceuticals, Inc. include SORBEX(TM) SOFT SPONGE and REDI-RELEASE ABSORBENT DRESSING.