Orthomatics, Inc.
Country not established
- Devices
- 1
What Orthomatics, Inc. makes
Orthomatics, Inc. manufactures the Orthoslendizer, a device designed for orthopedic applications, likely used in the reduction or alignment of bone fractures or joint deformities.
The company’s portfolio is regulated under FDA Class I devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Orthoslenderizer Ref K111249
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthomatics, Inc. have in the registry?
The registry currently lists 1 device for Orthomatics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthomatics, Inc.'s devices?
Among its 1 most recently registered device, Orthomatics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthomatics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthomatics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Orthomatics, Inc. in the registry?
The most recently registered devices listed for Orthomatics, Inc. include ORTHOSLENDERIZER.