Sulzer Calcitek, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Spline Dental Implant System - Spline Xi Implant Ref K981562
Regimes: 510(k) Registry: 510(k)Edosseous Dental Implant Ref K970127
Regimes: 510(k) Registry: 510(k)Spline Dental Implant System-Temporary Abutment Ref K982305
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Threadloc Dental Implant Systems Ref K964768
Regimes: 510(k) Registry: 510(k)Spline Engaging Shouldered Abutment System Ref K970752
Regimes: 510(k) Registry: 510(k)Spline Dental Implant System Ref K010073
Regimes: 510(k) Registry: 510(k)Removable Cuff Abutment Ref K984536
Regimes: 510(k) Registry: 510(k)Variable Parallel Pin Ref K973521
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sulzer Calcitek, Inc. have in the registry?
The registry currently lists 9 devices for Sulzer Calcitek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sulzer Calcitek, Inc.'s devices?
Among its 9 most recently registered devices, Sulzer Calcitek, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Sulzer Calcitek, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Sulzer Calcitek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sulzer Calcitek, Inc. in the registry?
The most recently registered devices listed for Sulzer Calcitek, Inc. include SPLINE DENTAL IMPLANT SYSTEM - SPLINE XI IMPLANT, EDOSSEOUS DENTAL IMPLANT, SPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENT and TEMPORARY GINGIVAL CUFF AND IMPRESSION POST AND IMPLANT ANALOG.