Digitek Dental Solutions Limited
ChinaFDA applicant, unverified
- Devices
- 1
What Digitek Dental Solutions Limited makes
Digitek Dental Solutions Limited manufactures dental abutments made from titanium, used as connectors between dental implants and prosthetic crowns or bridges to restore oral function and aesthetics.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Digitek Titanium Abutment Ref K141970
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digitek Dental Solutions Limited have in the registry?
The registry currently lists 1 device for Digitek Dental Solutions Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digitek Dental Solutions Limited's devices?
Among its 1 most recently registered device, Digitek Dental Solutions Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Digitek Dental Solutions Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Digitek Dental Solutions Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digitek Dental Solutions Limited in the registry?
The most recently registered devices listed for Digitek Dental Solutions Limited include DIGITEK TITANIUM ABUTMENT.