Medical Device Manufacturer · SE , Sweden

Abigo Medical AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Abigo Medical AB has 5 FDA 510(k) cleared medical devices. Based in Sweden, SE.

Historical record: 5 cleared submissions from 1992 to 2017. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.

Abigo Medical AB is one of 102 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Abigo Medical AB

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 14, 2026