Enhatch Orthopaedics, LLC
Country not established
- Devices
- 1
What Enhatch Orthopaedics, LLC makes
Enhatch Orthopaedics, LLC designs patient- and technique-specific humeral devices, likely intended for orthopaedic applications such as shoulder surgery or fracture fixation.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Enhatch Orthopaedics, LLC have in the registry?
The registry currently lists 1 device for Enhatch Orthopaedics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enhatch Orthopaedics, LLC's devices?
Among its 1 most recently registered device, Enhatch Orthopaedics, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Enhatch Orthopaedics, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Enhatch Orthopaedics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Enhatch Orthopaedics, LLC in the registry?
The most recently registered devices listed for Enhatch Orthopaedics, LLC include ENHATCH ORTHOPAEDICS PATIENT/TECHNIQUE-SPECIFIC HUMERAL.