Deheer Orthopedics
Country not established FDA establishment FEI 3030149892
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
Company details
- FDA FEI number
- 3030149892
- Address
- 387 Ridge Point Drive, Carmel, IN, 46032
Frequently asked questions
How many devices does DEHEER ORTHOPEDICS have in the registry?
The registry currently lists 1 device for DEHEER ORTHOPEDICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list DEHEER ORTHOPEDICS's devices?
Among its 1 most recently registered device, DEHEER ORTHOPEDICS has devices listed in FDA GUDID (1 device).
What risk classes do DEHEER ORTHOPEDICS's devices fall under?
Among its 1 most recently registered device, the classes recorded for DEHEER ORTHOPEDICS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from DEHEER ORTHOPEDICS in the registry?
The most recently registered devices listed for DEHEER ORTHOPEDICS include Baumann GRS Kit BGRS-KIT-001.