Alphamedix, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Versablade Ref K852633
Regimes: 510(k) Registry: 510(k)Versatome I Ref K820008
Regimes: 510(k) Registry: 510(k)Glomark Ref K830703
Regimes: 510(k) Registry: 510(k)Versaphage Ref K851272
Regimes: 510(k) Registry: 510(k)Alphamedix I/A Hand-Piece, 500-001 Ref K830812
Regimes: 510(k) Registry: 510(k)Disposable Surgical Garments Ref K820363
Regimes: 510(k) Registry: 510(k)Versablade Ref K852706
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alphamedix, Inc. have in the registry?
The registry currently lists 7 devices for Alphamedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alphamedix, Inc.'s devices?
Among its 7 most recently registered devices, Alphamedix, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Alphamedix, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Alphamedix, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alphamedix, Inc. in the registry?
The most recently registered devices listed for Alphamedix, Inc. include VERSABLADE, VERSATOME I, GLOMARK and VERSAPHAGE.