U.S. Implant Solutions, LLC
Country not established
- Devices
- 1
What U.S. Implant Solutions, LLC makes
U.S. Implant Solutions, LLC manufactures the Universal Compression Fracture Repair System, a device designed for internal fixation of compression fractures, likely in spinal or long-bone applications.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The system is listed in the U.S. regulatory registry, adhering to U.S. medical device compliance standards.
Catalogue
Universal Compression Fracture Repair System Ref K081813
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Implant Solutions, LLC have in the registry?
The registry currently lists 1 device for U.S. Implant Solutions, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Implant Solutions, LLC's devices?
Among its 1 most recently registered device, U.S. Implant Solutions, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do U.S. Implant Solutions, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for U.S. Implant Solutions, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Implant Solutions, LLC in the registry?
The most recently registered devices listed for U.S. Implant Solutions, LLC include UNIVERSAL COMPRESSION FRACTURE REPAIR SYSTEM.