Largent Health, LLC
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
FiteBac CC OrthoSeal Ref K210115
Regimes: 510(k) Registry: 510(k)FiteBac Antimicrobial Cavity Cleanser Ref K200614
Regimes: 510(k) Registry: 510(k)FiteBac Cavity Cleanser Ref K190271
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Largent Health, LLC have in the registry?
The registry currently lists 3 devices for Largent Health, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Largent Health, LLC's devices?
Among its 3 most recently registered devices, Largent Health, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Largent Health, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Largent Health, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Largent Health, LLC in the registry?
The most recently registered devices listed for Largent Health, LLC include FiteBac CC OrthoSeal, FiteBac Antimicrobial Cavity Cleanser and FiteBac Cavity Cleanser.