Triad Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Triad Medical, Inc. have in the registry?
The registry currently lists 2 devices for Triad Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Triad Medical, Inc.'s devices?
Among its 2 most recently registered devices, Triad Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Triad Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Triad Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Triad Medical, Inc. in the registry?
The most recently registered devices listed for Triad Medical, Inc. include HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED, MODEL 7.3MM and HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED, VERSION 2.