Additive Implants, Inc.
United StatesFDA applicant, unverified
- Devices
- 473
What Additive Implants, Inc. makes
Additive Implants, Inc. manufactures metallic spinal interbody fusion cages, reusable orthopaedic positioning instruments, and reusable implant inserter/extractors. Their product line also includes reusable instrument trays and surgical mallets, designed for spinal and orthopaedic procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer is based in the United States.
Catalogue
Search and filter all 473 devicesShowing 1-50 of 473
Frequently asked questions
How many devices does Additive Implants, Inc. have in the registry?
The registry currently lists 473 devices for Additive Implants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Additive Implants, Inc.'s devices?
Among its 50 most recently registered devices, Additive Implants, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Additive Implants, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Additive Implants, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Additive Implants, Inc. in the registry?
The most recently registered devices listed for Additive Implants, Inc. include SureMAX 1, SureMAX-X 1 and SureMAX-SA 1.