SINTX Technologies Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3005032068
- Devices
- 3,032
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 3,032 devicesShowing 1-50 of 3,032
Company details
- FDA FEI number
- 3005032068
- Address
- 1885 W 2100 S, Salt Lake City, UT, 84119
Frequently asked questions
How many devices does SINTX Technologies Inc. have in the registry?
The registry currently lists 3032 devices for SINTX Technologies Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SINTX Technologies Inc.'s devices?
Among its 50 most recently registered devices, SINTX Technologies Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do SINTX Technologies Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for SINTX Technologies Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SINTX Technologies Inc. in the registry?
The most recently registered devices listed for SINTX Technologies Inc. include SiNAPTIC Osteotomy Wedge System Inserter - Rev. 0, SiNAPTIC Osteotomy Wedge System Tamp - Rev. 0, SiNAPTIC Osteotomy Wedge System Cotton Trial - Rev. 0 and SiNAPTIC Osteotomy Wedge System Evans Wedge - Rev. 1.