Glw Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CREED™ Cannulated Screws Ref K200291
Regimes: 510(k) Registry: 510(k)Apollo Ankle Fracture Plating System Ref K213005
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glw Medical, Inc. have in the registry?
The registry currently lists 2 devices for Glw Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glw Medical, Inc.'s devices?
Among its 2 most recently registered devices, Glw Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Glw Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Glw Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glw Medical, Inc. in the registry?
The most recently registered devices listed for Glw Medical, Inc. include CREED™ Cannulated Screws and Apollo Ankle Fracture Plating System.