Dental Ventures of America, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Dental Ventures of America, Inc. makes
Dental Ventures of America, Inc. manufactures dental alloys and materials for crowns, bridges, and restorative procedures, including nonprecious crown and bridge alloys, resin-based powder-liquid systems for dental composites, and ultrasonic scaling systems for dental hygiene.
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
Ms Nonprecious Crown & Bridge Alloy Ref K842377
Regimes: 510(k) Registry: 510(k)C&B Resin Plus Powder/Liquid, Models Retemp A2, A3, A3.5, Cl, Retemp B2, B3, C2, D3, Wh, Retemp Mo Ref K000894
Regimes: 510(k) Registry: 510(k)Piezomatic Ultrasonic Scaler (System S) Ref K780808
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dental Ventures of America, Inc. have in the registry?
The registry currently lists 3 devices for Dental Ventures of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dental Ventures of America, Inc.'s devices?
Among its 3 most recently registered devices, Dental Ventures of America, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dental Ventures of America, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dental Ventures of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dental Ventures of America, Inc. in the registry?
The most recently registered devices listed for Dental Ventures of America, Inc. include MS NONPRECIOUS CROWN & BRIDGE ALLOY, C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO and PIEZOMATIC ULTRASONIC SCALER (SYSTEM S).