Medical Device Manufacturer · US , Aubrey , TX

Sectra AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Sectra AB has 5 FDA 510(k) cleared medical devices. Based in Aubrey, US.

Latest FDA clearance: Apr 2024. Active since 2000. Primary specialty: Radiology.

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

Regulatory submissions have been managed by Peter Altman and Medical Device Regulatory Services.

Sectra AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sectra AB

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 10, 2026