Amedica Corp.
United StatesFDA applicant, unverified
- Devices
- 17
What Amedica Corp. makes
Amedica Corp. manufactures single-use internal spinal fixation procedure kits and sterile bone-screw systems for spinal stabilization. Their portfolio includes vertebral body prostheses designed for spinal fusion procedures, primarily under the Valeo Spacer System and Valeo Fusion System brands.
The company’s devices are classified under FDA categories Class I and Class II, with records maintained in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Amedica Corp. have in the registry?
The registry currently lists 17 devices for Amedica Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amedica Corp.'s devices?
Among its 17 most recently registered devices, Amedica Corp. has devices listed in FDA 510(k) (17 devices).
What risk classes do Amedica Corp.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Amedica Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amedica Corp. in the registry?
The most recently registered devices listed for Amedica Corp. include VALEO CERVICAL PLATE SYSTEM, VALEO PEDICLE SCREW SPINAL SYSTEM, PHANTOM PLUS CERAMIC CAGE SYSTEM and MODIFICATION TO VALEO VBR.