AmFab Co., LLC
Also registered as Am Fab, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1831748
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Am Fab Side Rails Model 5000 Ref K852890
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1831748
- Address
- 8850 M-89 Hwy, Richland, MI, 49083
Frequently asked questions
How many devices does AmFab Co., LLC have in the registry?
The registry currently lists 1 device for AmFab Co., LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list AmFab Co., LLC's devices?
Among its 1 most recently registered device, AmFab Co., LLC has devices listed in FDA 510(k) (1 device).
What risk classes do AmFab Co., LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for AmFab Co., LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from AmFab Co., LLC in the registry?
The most recently registered devices listed for AmFab Co., LLC include AM FAB SIDE RAILS MODEL 5000.