Syntex Dental Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Syntex Dental Products, Inc. makes
Syntex Dental Products, Inc. manufactures precapsuled dental amalgam for cavity restorations, a vibratory endodontic system for root canal procedures, and sterile water systems for dental unit irrigation.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Precapsuled Dental Amalgam Ref K822610
Regimes: 510(k) Registry: 510(k)Vibratory Endodontic System Ref K832378
Regimes: 510(k) Registry: 510(k)Sterile Water System Ref K823230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Syntex Dental Products, Inc. have in the registry?
The registry currently lists 3 devices for Syntex Dental Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syntex Dental Products, Inc.'s devices?
Among its 3 most recently registered devices, Syntex Dental Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Syntex Dental Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Syntex Dental Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Syntex Dental Products, Inc. in the registry?
The most recently registered devices listed for Syntex Dental Products, Inc. include PRECAPSULED DENTAL AMALGAM, VIBRATORY ENDODONTIC SYSTEM and STERILE WATER SYSTEM.