Vertiflex, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 23
What Vertiflex, Inc. makes
Vertiflex, Inc. manufactures spinal fixation and decompression devices, including spinal screw systems, spinoous process fixation plates, vertebral body replacement systems, and direct decompression tools for surgical spinal interventions.
The company’s portfolio consists of Class II medical devices, all of which are cleared via the FDA’s 510(k) pathway. These devices are based in the United States.
Catalogue
Search and filter all 23 devicesCompany details
- DUNS number
- 005235436
Frequently asked questions
How many devices does VERTIFLEX, INC. have in the registry?
The registry currently lists 23 devices for VERTIFLEX, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VERTIFLEX, INC.'s devices?
Among its 23 most recently registered devices, VERTIFLEX, INC. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do VERTIFLEX, INC.'s devices fall under?
Among its 23 most recently registered devices, the classes recorded for VERTIFLEX, INC.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from VERTIFLEX, INC. in the registry?
The most recently registered devices listed for VERTIFLEX, INC. include Superion Retractor 100-9126, Superion Interspinous Spacer 14mm, Superion Sterilization Tray 100-9119 and Superion Interspinous Spacer 8mm.