Vertelink Corporation
United StatesFDA applicant, unverified
- Devices
- 3
What Vertelink Corporation makes
Vertelink Corporation manufactures spinal fixation hardware, including the Kobra Spinal Fixation System for orthopedic stabilization, and vascular access tools like the Pathway Access Sheath Catheter for guiding and securing catheters in medical procedures.
The company’s products are regulated as Class II devices under the FDA’s 510(k) pathway and are listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
Vertelink Kobra Spinal Fixation System Ref K032102
Regimes: 510(k) Registry: 510(k)Pathway Access Sheath Catheter Ref K030734
Regimes: 510(k) Registry: 510(k)Pathway Access Sheath Catheter Ref K030662
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vertelink Corporation have in the registry?
The registry currently lists 3 devices for Vertelink Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertelink Corporation's devices?
Among its 3 most recently registered devices, Vertelink Corporation has devices listed in FDA 510(k) (3 devices).
What risk classes do Vertelink Corporation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vertelink Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertelink Corporation in the registry?
The most recently registered devices listed for Vertelink Corporation include VERTELINK KOBRA SPINAL FIXATION SYSTEM and PATHWAY ACCESS SHEATH CATHETER.