Ignite Orthopedics, Inc.
Also registered as Ignite Orthopedics, LLC
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ignite Stemless Anatomic Shoulder System Ref K203108
Regimes: 510(k) Registry: 510(k)Ignite Anatomic Shoulder System Ref K202716
Regimes: 510(k) Registry: 510(k)Revolution Radial Head Ref K183618
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ignite Orthopedics, Inc. have in the registry?
The registry currently lists 3 devices for Ignite Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ignite Orthopedics, Inc.'s devices?
Among its 3 most recently registered devices, Ignite Orthopedics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ignite Orthopedics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ignite Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ignite Orthopedics, Inc. in the registry?
The most recently registered devices listed for Ignite Orthopedics, Inc. include Ignite Stemless Anatomic Shoulder System, Ignite Anatomic Shoulder System and Revolution Radial Head.