Medical Device Manufacturer · US , Garner, , NC

Curasan AG - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2002

Total

Cleared

Denied

Curasan AG has 10 FDA 510(k) cleared medical devices. Based in Garner,, US.

Historical record: 10 cleared submissions from 2002 to 2018. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Curasan AG

10 devices

1-10 of 10

CURASAN OSSEOLIVE DENTAL

REVOIS IMPLANT SYSTEM

MODIFICATION TO CERASORB ORTHO

Curasan AG - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Curasan AG

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