Harmos Orthopaedics, Inc.
Country not established
- Devices
- 1
What Harmos Orthopaedics, Inc. makes
Harmos Orthopaedics, Inc. manufactures the Great Toe Implant System, a surgical device designed for the replacement or augmentation of the first metatarsophalangeal joint in the foot.
The company’s portfolio is regulated under FDA’s Class II device classification, with devices listed via the 510(k) clearance pathway. Harmos Orthopaedics, Inc. is based in the United States.
Catalogue
Great Toe Implant System Ref K014164
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Harmos Orthopaedics, Inc. have in the registry?
The registry currently lists 1 device for Harmos Orthopaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harmos Orthopaedics, Inc.'s devices?
Among its 1 most recently registered device, Harmos Orthopaedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Harmos Orthopaedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Harmos Orthopaedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harmos Orthopaedics, Inc. in the registry?
The most recently registered devices listed for Harmos Orthopaedics, Inc. include GREAT TOE IMPLANT SYSTEM.