Enhatch, Inc.
Country not established
- Devices
- 1
What Enhatch, Inc. makes
Enhatch, Inc. makes orthopedic devices, including patient-specific instrumentation for knee procedures.
The company's portfolio, which includes devices such as the United Orthopedic Knee Patient Specific Instrumentation, is regulated as Class II devices and is listed in the FDA 510(k) registry. Enhatch, Inc. is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Enhatch, Inc. have in the registry?
The registry currently lists 1 device for Enhatch, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enhatch, Inc.'s devices?
Among its 1 most recently registered device, Enhatch, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Enhatch, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Enhatch, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Enhatch, Inc. in the registry?
The most recently registered devices listed for Enhatch, Inc. include United Orthopedic Knee Patient Specific Instrumentation.