Diamodent
United Statesfrom the FDA registration address FDA FEI 3002832763
- Devices
- 423
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Diamodent makes
Diamodent manufactures dental implant suprastructures, including permanent and temporary preformed types, as well as reusable and single-use variants. Their portfolio also includes dental implant abutment analogs for laboratory use, dental prosthesis/implant abutment screws, surgical screwdrivers, torque wrench adaptors, and reusable surgical instrument handles. These products are designed for dental procedures requiring precision fitting and secure attachment of implant components.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are regulated under U.S. medical device laws, ensuring compliance with applicable standards for dental implants and surgical instruments. The manufacturer is based in the United States.
Catalogue
Search and filter all 423 devicesShowing 1-50 of 423
Company details
- FDA FEI number
- 3002832763
- Address
- 35577 Beach Road, Dana Point, CA, 92624
Frequently asked questions
How many devices does Diamodent have in the registry?
The registry currently lists 423 devices for Diamodent. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diamodent's devices?
Among its 50 most recently registered devices, Diamodent has devices listed in FDA GUDID (50 devices).
What risk classes do Diamodent's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Diamodent's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diamodent in the registry?
The most recently registered devices listed for Diamodent include Diamodent AK1001, Diamodent P510, Diamodent AB1010 and Diamodent R700.