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Camber Spine Technologies

Also registered as CAMBER SPINE TECHNOLOGIES, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3010197239

Devices
5,148
Registrations
FDA
FDA recalls
0

What Camber Spine Technologies makes

The company manufactures spinal fixation hardware, including non-bioabsorbable screws, metallic and polymeric interbody fusion cages, spinal plates, and reusable instrument trays. It also produces spinal implant trial devices and ophthalmic surgical forceps for handling implants. Systems like the SPIRA®-T and ALTIVO™ are designed for anterior and lateral spinal fusion procedures, while the ORTHROS and Ti-Diagon devices support specific spinal stabilization applications.

These devices are regulated under FDA Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable U.S. medical device regulations.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5,148

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Company details

FDA FEI number
3010197239
Address
501 Allendale Rd, King of Prussia, PA, 19406

Frequently asked questions

How many devices does CAMBER SPINE TECHNOLOGIES have in the registry?

The registry currently lists 5148 devices for CAMBER SPINE TECHNOLOGIES. Devices recorded under merged duplicate company entries are counted once.

Which registries list CAMBER SPINE TECHNOLOGIES's devices?

Among its 50 most recently registered devices, CAMBER SPINE TECHNOLOGIES has devices listed in FDA GUDID (50 devices).

What risk classes do CAMBER SPINE TECHNOLOGIES's devices fall under?

Among its 50 most recently registered devices, the classes recorded for CAMBER SPINE TECHNOLOGIES's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from CAMBER SPINE TECHNOLOGIES in the registry?

The most recently registered devices listed for CAMBER SPINE TECHNOLOGIES include ORTHROS MIS CM-117-06, ORTHROS CC-117-50, SPIRA®-T Integrated Fixation System SPT-2609-1515 and ALTIVO™ Anterior Cervical Fixation System FCP-2430.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.