DMG America LLC
United Statesfrom the FDA registration address FDA establishment FEI 2244812
- Devices
- 113
- Registrations
- FDA
- FDA recalls
- 0
What DMG America LLC makes
DMG America LLC makes dental products, including dental amalgam, dentifrice, dental coatings, and restorative materials. Their products include dental amalgam mixers, varnishes, and composite resins, as well as gingival retraction kits and root canal post kits.
The company's portfolio is regulated as Class I and Class II devices and is listed in the FDA UDI registry. The company is based in the US.
Catalogue
Search and filter all 113 devicesShowing 1-50 of 113
Company details
- FDA FEI number
- 2244812
- Address
- 242 S Dean St, ENGLEWOOD, NJ, 07631
Frequently asked questions
How many devices does DMG America LLC have in the registry?
The registry currently lists 113 devices for DMG America LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list DMG America LLC's devices?
Among its 50 most recently registered devices, DMG America LLC has devices listed in FDA GUDID (50 devices).
What risk classes do DMG America LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for DMG America LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from DMG America LLC in the registry?
The most recently registered devices listed for DMG America LLC include DMG 220600, Ultra Dispersed Phase High Copper 55064, Kolorz Prophylaxis Paste 788406 and ZenithDental Premium Dispersed Phase 61206.