Infront Medical, LLC
Country not established
- Devices
- 32
What Infront Medical, LLC makes
Infront Medical, LLC manufactures polymeric spinal interbody fusion cages, designed for use in spinal fusion procedures to stabilize the spine and promote bone growth between vertebrae. These devices are intended to provide structural support and facilitate healing in patients with degenerative disc disease, spinal instability, or other spinal pathologies requiring surgical intervention.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) and Unique Device Identification (UDI) pathways. These devices are listed in the FDA’s regulatory databases, ensuring compliance with U.S. medical device standards. The manufacturer operates from the United States.
Catalogue
Search and filter all 32 devicesCompany details
- DUNS number
- 079944908
- [email protected]
- Phone
- 1 (888) 515-2532
Frequently asked questions
How many devices does Infront Medical, LLC have in the registry?
The registry currently lists 32 devices for Infront Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Infront Medical, LLC's devices?
Among its 32 most recently registered devices, Infront Medical, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (31 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Infront Medical, LLC's devices fall under?
Among its 32 most recently registered devices, the classes recorded for Infront Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Infront Medical, LLC in the registry?
The most recently registered devices listed for Infront Medical, LLC include InFront 003-BB8E, InFront 003-AB07, InFront 004-CA0D and InFront 004-CA48.