Knopf Assoc, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prosthoflex Ref K942562
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Knopf Assoc, Inc. have in the registry?
The registry currently lists 1 device for Knopf Assoc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Knopf Assoc, Inc.'s devices?
Among its 1 most recently registered device, Knopf Assoc, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Knopf Assoc, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Knopf Assoc, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Knopf Assoc, Inc. in the registry?
The most recently registered devices listed for Knopf Assoc, Inc. include PROSTHOFLEX.