Kat Implants, LLC
United StatesFDA applicant, unverified FDA FEI 3007728094
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Kat Implants System One-Piece Implants 2.5X10 Ref K112758
Regimes: 510(k) Registry: 510(k)Kat Implant System Ref K083544
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007728094
- Address
- 222 International Drive, No. 185, Portsmouth, NH, 03801
Frequently asked questions
How many devices does Kat Implants, LLC have in the registry?
The registry currently lists 3 devices for Kat Implants, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kat Implants, LLC's devices?
Among its 3 most recently registered devices, Kat Implants, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Kat Implants, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Kat Implants, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kat Implants, LLC in the registry?
The most recently registered devices listed for Kat Implants, LLC include STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,, KAT IMPLANTS SYSTEM ONE-PIECE IMPLANTS 2.5X10 and KAT IMPLANT SYSTEM.