Odon Lifetechnology
FranceFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Snare, Flexible Ref K002927
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odon Lifetechnology have in the registry?
The registry currently lists 1 device for Odon Lifetechnology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odon Lifetechnology's devices?
Among its 1 most recently registered device, Odon Lifetechnology has devices listed in FDA 510(k) (1 device).
What risk classes do Odon Lifetechnology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Odon Lifetechnology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odon Lifetechnology in the registry?
The most recently registered devices listed for Odon Lifetechnology include SNARE, FLEXIBLE.