Omsbar, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Omsbar, Ltd. makes
Omsbar, Ltd. manufactures the ORTHOVIEW, a medical imaging device designed for orthopedic applications, likely used to visualize bone structures or surgical planning in real-time or post-procedure contexts.
The ORTHOVIEW is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Orthoview Ref K032401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omsbar, Ltd. have in the registry?
The registry currently lists 1 device for Omsbar, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omsbar, Ltd.'s devices?
Among its 1 most recently registered device, Omsbar, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Omsbar, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omsbar, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omsbar, Ltd. in the registry?
The most recently registered devices listed for Omsbar, Ltd. include ORTHOVIEW.