Facet-Link, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Facet-Link, Inc. makes
Facet-Link, Inc. manufactures the Facet-Link Stabilization Platform, a device designed for spinal stabilization procedures, and the FACET SCREW SYSTEM, which includes screws and associated hardware for spinal fixation. These products are intended for use in surgical interventions to support and align vertebrae in the spine.
The company’s devices are classified under Class II (U) in the U.S. regulatory framework and are listed under the FDA’s 510(k) clearance process. The portfolio is regulated and tracked within the United States, where Facet-Link, Inc. is based.
Catalogue
Facet-Link Stabilization Platform Ref K150223
510(k) 510(k)Facet Screw System Ref K123497
510(k) 510(k)
Frequently asked questions
How many devices does Facet-Link, Inc. have in the registry?
The registry currently lists 2 devices for Facet-Link, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Facet-Link, Inc.'s devices?
Among its 2 most recently registered devices, Facet-Link, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Facet-Link, Inc. in the registry?
The most recently registered devices listed for Facet-Link, Inc. include Facet-Link Stabilization Platform and FACET SCREW SYSTEM.