Centrix, Inc.
United StatesFDA applicant, unverified FDA FEI 1281412
- Devices
- 280
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Centrix, Inc. makes
Centrix, Inc. manufactures dental composite resins, temporary crown and bridge resins, and silicone impression materials. The company also produces various dental application tools, including single-use injection cannulas, single-component cartridge-plunging applicators, non-medicated gingival retraction cords, and cavity varnishes.
The company is based in the United States, and its product portfolio includes devices classified as Class I, Class II, and U. These devices are listed in the FDA 510(k) and FDA UDI regulatory registries.
Catalogue
Search and filter all 280 devicesShowing 1-50 of 280
Company details
- FDA FEI number
- 1281412
- DUNS number
- 053707303
- Address
- 770 River Rd, Shelton, CT, 06484
Frequently asked questions
How many devices does CENTRIX, INC. have in the registry?
The registry currently lists 280 devices for CENTRIX, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CENTRIX, INC.'s devices?
Among its 50 most recently registered devices, CENTRIX, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do CENTRIX, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for CENTRIX, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from CENTRIX, INC. in the registry?
The most recently registered devices listed for CENTRIX, INC. include PHOSPHORIC-ACID ETCHING GEL, Accudose 920141, EZ 914040 and Centrix Endo Kit 360053.