Genesis Orthopedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Go Intramedullary Nail Locking Screw Ref K954511
Regimes: 510(k) Registry: 510(k)Go Universalk-Wire Fluted Drill Ref K954543
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genesis Orthopedics, Inc. have in the registry?
The registry currently lists 2 devices for Genesis Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genesis Orthopedics, Inc.'s devices?
Among its 2 most recently registered devices, Genesis Orthopedics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Genesis Orthopedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Genesis Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genesis Orthopedics, Inc. in the registry?
The most recently registered devices listed for Genesis Orthopedics, Inc. include GO INTRAMEDULLARY NAIL LOCKING SCREW and GO UNIVERSALK-WIRE FLUTED DRILL.