General Dental Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What General Dental Products, Inc. makes
General Dental Products, Inc. manufactures silicone splinting materials and poly-tone denture base resins, which are used in dental restorations and prosthetics.
These products are regulated under FDA Class I and Class II categories, with authorisation via the 510(k) pathway, and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Silicone Splinting Material Ref K840113
Regimes: 510(k) Registry: 510(k)Poly-Tone Denture Base Resin Ref K823568
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Dental Products, Inc. have in the registry?
The registry currently lists 2 devices for General Dental Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Dental Products, Inc.'s devices?
Among its 2 most recently registered devices, General Dental Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do General Dental Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for General Dental Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Dental Products, Inc. in the registry?
The most recently registered devices listed for General Dental Products, Inc. include SILICONE SPLINTING MATERIAL and POLY-TONE DENTURE BASE RESIN.