Laboratoire Villanova
FranceFDA applicant, unverified
- Devices
- 1
What Laboratoire Villanova makes
Laboratoire Villanova manufactures the HA Orbital Implant, a device designed for orbital reconstruction or augmentation in ophthalmic surgery.
The HA Orbital Implant is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ha Orbital Implant Ref K021643
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratoire Villanova have in the registry?
The registry currently lists 1 device for Laboratoire Villanova. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratoire Villanova's devices?
Among its 1 most recently registered device, Laboratoire Villanova has devices listed in FDA 510(k) (1 device).
What risk classes do Laboratoire Villanova's devices fall under?
Among its 1 most recently registered device, the classes recorded for Laboratoire Villanova's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laboratoire Villanova in the registry?
The most recently registered devices listed for Laboratoire Villanova include HA ORBITAL IMPLANT.