Ortho-J, Inc.
Country not established
- Devices
- 1
What Ortho-J, Inc. makes
Ortho-J, Inc. manufactures the BEK-JS-004 device, which is classified as a Class I medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ortho-J, Inc. Bek-Js-004 Ref K891917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ortho-J, Inc. have in the registry?
The registry currently lists 1 device for Ortho-J, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortho-J, Inc.'s devices?
Among its 1 most recently registered device, Ortho-J, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ortho-J, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ortho-J, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ortho-J, Inc. in the registry?
The most recently registered devices listed for Ortho-J, Inc. include ORTHO-J, INC. BEK-JS-004.