Restore Surgical LLC
Country not established
- Devices
- 192
What Restore Surgical LLC makes
Restore Surgical LLC manufactures orthopaedic bone screws made from titanium, including cannulated designs with threaded and headless variants. These devices are intended for use in surgical fixation of bone, such as fracture stabilization or joint reconstruction, and are supplied in non-sterile form.
The company’s products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.
Catalogue
Search and filter all 192 devicesShowing 1-50 of 192
Company details
- DUNS number
- 792932626
Frequently asked questions
How many devices does Restore Surgical LLC have in the registry?
The registry currently lists 192 devices for Restore Surgical LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Restore Surgical LLC's devices?
Among its 50 most recently registered devices, Restore Surgical LLC has devices listed in FDA GUDID (50 devices).
What risk classes do Restore Surgical LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Restore Surgical LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Restore Surgical LLC in the registry?
The most recently registered devices listed for Restore Surgical LLC include Mini Cannulated Titanium Headed and Headless Screw Set IC2518, Mini Cannulated Titanium Headed and Headless Screw Set IC3034, Mini Cannulated Titanium Headed and Headless Screw Set IC3032 and Mini Cannulated Titanium Headed and Headless Screw Set IC2532.