Medical Device Manufacturer · FR , France

Micro-Mega - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

Micro-Mega has 2 FDA 510(k) cleared medical devices. Based in France, FR.

Historical record: 2 cleared submissions from 1994 to 1997. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Micro-Mega Filter by specialty or product code using the sidebar.

Micro-Mega is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Micro-Mega

2 devices

1-2 of 2