Medical Device Manufacturer · FR , Le Touquet

Laboratoire Villanova - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Recent clearances: HA ORBITAL IMPLANT

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Laboratoire Villanova Ophthalmic ✕

1 devices

1-1 of 1

Cleared Dec 13, 2002

HA ORBITAL IMPLANT

Ophthalmic · 207d