Veos, Ltd.
Country not established
- Devices
- 1
What Veos, Ltd. makes
Veos, Ltd. manufactures the OVES Cervical Cap, a medical device designed for cervical support and stabilization in specific clinical applications.
The OVES Cervical Cap 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
Oves Cervical Cap Ref K993953
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veos, Ltd. have in the registry?
The registry currently lists 1 device for Veos, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veos, Ltd.'s devices?
Among its 1 most recently registered device, Veos, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Veos, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Veos, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veos, Ltd. in the registry?
The most recently registered devices listed for Veos, Ltd. include OVES CERVICAL CAP.