Inosys, Inc.
United Statesfrom the FDA registration address FDA FEI 3022316560
- Devices
- 267
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Inosys, Inc. makes
Inosys, Inc. manufactures dental implant components and related surgical kits, including permanent and temporary preformed suprastructures, two-piece screw endosteal dental implants, single-use abutment screw analogs, dental implant analogs, and reusable non-medicated surgical procedure kits for dental and maxillofacial procedures. Specific examples of their products include Pick-Up Impression Coping, Transfer Impression Coping, and various components of the PRIMUS Implant System and Bone Level Fixture.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) registry. Inosys, Inc. is based in the United States.
Catalogue
Search and filter all 267 devicesShowing 1-50 of 267
Company details
- FDA FEI number
- 3022316560
- DUNS number
- 101803383
- Address
- 545 W 45th St Fl 11, New York, NY, 10036
Frequently asked questions
How many devices does Inosys, Inc. have in the registry?
The registry currently lists 267 devices for Inosys, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inosys, Inc.'s devices?
Among its 50 most recently registered devices, Inosys, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Inosys, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Inosys, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inosys, Inc. in the registry?
The most recently registered devices listed for Inosys, Inc. include (INOSS System) INOSS Fixture IBF-3708S, (INOSS System) INOSS Fixture IBF-3710S, (INOSS System) INOSS Fixture IBF-3711S and (INOSS System) INOSS Fixture IBF-3713S.