Promedex, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Promedex, Inc. makes
Promedex, Inc. makes Varicoscreen(TM), Seminor, and Promoglass(TM) sunglasses (non-prescription).
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Varicoscreen(Tm) Ref K900404
Regimes: 510(k) Registry: 510(k)Seminor Ref K905764
Regimes: 510(k) Registry: 510(k)Promoglass(Tm) Sunglasses (Non-Prescription) Ref K914407
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promedex, Inc. have in the registry?
The registry currently lists 3 devices for Promedex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promedex, Inc.'s devices?
Among its 3 most recently registered devices, Promedex, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Promedex, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Promedex, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promedex, Inc. in the registry?
The most recently registered devices listed for Promedex, Inc. include VARICOSCREEN(TM), SEMINOR and PROMOGLASS(TM) SUNGLASSES (NON-PRESCRIPTION).