Frontier Devices, Inc.
Country not established
- Devices
- 1
What Frontier Devices, Inc. makes
Frontier Devices, Inc. manufactures craniomaxillofacial, cranial closure, orthognathic, mandible reconstruction, and mesh systems for surgical applications.
These devices are Class II and listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Frontier Devices Craniomaxillofacial, Cranio Closure, Orthognathic, Mandible Reconstruction And Mesh Systems Ref K091812
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Frontier Devices, Inc. have in the registry?
The registry currently lists 1 device for Frontier Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Frontier Devices, Inc.'s devices?
Among its 1 most recently registered device, Frontier Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Frontier Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Frontier Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Frontier Devices, Inc. in the registry?
The most recently registered devices listed for Frontier Devices, Inc. include FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS.