Osteotek, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dunn Anterior Distraction System Ref K862755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteotek, Inc. have in the registry?
The registry currently lists 1 device for Osteotek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteotek, Inc.'s devices?
Among its 1 most recently registered device, Osteotek, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Osteotek, Inc. in the registry?
The most recently registered devices listed for Osteotek, Inc. include DUNN ANTERIOR DISTRACTION SYSTEM.