Linkspine, Inc.
Country not established
- Devices
- 592
What Linkspine, Inc. makes
The company manufactures spinal fixation instruments and implants, including non-sterile bone-screw and trans-facet-screw systems for internal spinal stabilization, as well as sterile polymeric spinal fusion cages. Their reusable surgical tools include bone taps, curettes, drill guides, and cannulated drill bits, designed for spinal procedures. The portfolio also covers specialized screwdrivers tailored for spinal applications.
These devices are classified under FDA categories Class I, Class II, and Unclassified (U), with all products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 592 devicesShowing 1-50 of 592
Company details
- DUNS number
- 067584601
- cs@linkspine.com
- Phone
- 1-410-772-5465
Frequently asked questions
How many devices does LINKSPINE, INC. have in the registry?
The registry currently lists 592 devices for LINKSPINE, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LINKSPINE, INC.'s devices?
Among its 50 most recently registered devices, LINKSPINE, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do LINKSPINE, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for LINKSPINE, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from LINKSPINE, INC. in the registry?
The most recently registered devices listed for LINKSPINE, INC. include CorticaLINK 80-4017/5025, VertebraLINK 84-0005/1400, VertebraLINK 84-0012/1100 and VertebraLINK 84-0005/0600.