Medical Device Manufacturer · FR , Antony

Moria SA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2002
5
Total
5
Cleared
0
Denied

Moria SA has 5 FDA 510(k) cleared medical devices. Based in Antony, FR.

Historical record: 5 cleared submissions from 2002 to 2017. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Moria SA Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Moria SA

5 devices
1-5 of 5
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All5 Ophthalmic 5