Medical Device Manufacturer · SE , Malmo

Ospol AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008

1

Total

1

Cleared

0

Denied

Ospol AB has 1 FDA 510(k) cleared medical devices. Based in Malmo, SE.

Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Dental.

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

Ospol AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ospol AB

1 devices

1-1 of 1

Cleared Mar 24, 2008

DENTAL IMPLANT, DENTAL ABUTMENT, ABUTMENT SCREW, COVER SCREW, HEALING ABUTMENT