Pentron Clinical
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Build-It Total Core Ref K102703
Regimes: 510(k) Registry: 510(k)Tempspan Clear Matrix Ref K120013
Regimes: 510(k) Registry: 510(k)Correct Plus 1 Ref K130920
Regimes: 510(k) Registry: 510(k)B1P Adhesive Ref K111431
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pentron Clinical have in the registry?
The registry currently lists 4 devices for Pentron Clinical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pentron Clinical's devices?
Among its 4 most recently registered devices, Pentron Clinical has devices listed in FDA 510(k) (4 devices).
What risk classes do Pentron Clinical's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pentron Clinical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pentron Clinical in the registry?
The most recently registered devices listed for Pentron Clinical include BUILD-IT TOTAL CORE, TEMPSPAN CLEAR MATRIX, CORRECT PLUS 1 and B1P ADHESIVE.