Spire Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dermabraders Ref K821485
Regimes: 510(k) Registry: 510(k)Micro-Sugical Power Instrument System Ref K802503
Regimes: 510(k) Registry: 510(k)Micro-Surgical Power Instrument System Ref K802463
Regimes: 510(k) Registry: 510(k)Micro Drills Ref K821486
Regimes: 510(k) Registry: 510(k)Micro-Surgical Power Instrument Sys. Ref K821487
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spire Medical, Inc. have in the registry?
The registry currently lists 5 devices for Spire Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spire Medical, Inc.'s devices?
Among its 5 most recently registered devices, Spire Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Spire Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Spire Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spire Medical, Inc. in the registry?
The most recently registered devices listed for Spire Medical, Inc. include DERMABRADERS, MICRO-SUGICAL POWER INSTRUMENT SYSTEM, MICRO-SURGICAL POWER INSTRUMENT SYSTEM and MICRO DRILLS.