Dentatus Usa Ltd.
Country not established FDA establishment FEI 2435118
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Tuf Link Silicone Reliner Ref K042931
510(k) 510(k)- 510(k) 510(k)
Dentatus Osciomat Ref K031793
510(k) 510(k)- 510(k) 510(k)
Company details
- FDA FEI number
- 2435118
- Address
- 50 Broadway, Hawthorne, NY, 10532
Frequently asked questions
How many devices does DENTATUS USA LTD. have in the registry?
The registry currently lists 4 devices for DENTATUS USA LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list DENTATUS USA LTD.'s devices?
Among its 4 most recently registered devices, DENTATUS USA LTD. has devices listed in FDA 510(k) (4 devices).
What risk classes do DENTATUS USA LTD.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for DENTATUS USA LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DENTATUS USA LTD. in the registry?
The most recently registered devices listed for DENTATUS USA LTD. include TUF LINK SILICONE RELINER, DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEM, DENTATUS OSCIOMAT and MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM.