Vertebron, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Vertebron, Inc. makes
Vertebron, Inc. manufactures spinal fixation systems including pedicle screw systems, cervical plate systems, and vertebral body replacement systems.
The company's products are Class II medical devices listed in the FDA 510(k) registry, and Vertebron is based in the US.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Vertebron, Inc. have in the registry?
The registry currently lists 11 devices for Vertebron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertebron, Inc.'s devices?
Among its 11 most recently registered devices, Vertebron, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Vertebron, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Vertebron, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertebron, Inc. in the registry?
The most recently registered devices listed for Vertebron, Inc. include MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM, VERTEBRON SCP CERVICAL PLATE SYSTEM, VERTEBRON VBR SYSTEM and MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM.