General A. Nitznick, D.M.D.
Country not established
- Devices
- 1
What General A. Nitznick, D.M.D. makes
General A. Nitznick, D.M.D. manufactures endosseous screw implants, which are designed for dental applications to anchor dental prosthetics within the jawbone. These devices are intended for use in fixed dental restorations, such as bridges or crowns, providing stable support for long-term oral rehabilitation.
The company’s endosseous screw implants fall under FDA Class II regulation and are listed via the 510(k) pathway. These devices are registered in the United States, where they must comply with applicable FDA requirements for dental implants. No additional international registries are referenced in the available data.
Catalogue
Endosseous Screw Implant Ref K820163
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General A. Nitznick, D.M.D. have in the registry?
The registry currently lists 1 device for General A. Nitznick, D.M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General A. Nitznick, D.M.D.'s devices?
Among its 1 most recently registered device, General A. Nitznick, D.M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do General A. Nitznick, D.M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for General A. Nitznick, D.M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General A. Nitznick, D.M.D. in the registry?
The most recently registered devices listed for General A. Nitznick, D.M.D. include ENDOSSEOUS SCREW IMPLANT.