Medical Device Manufacturer · US , Andover , MA

Capsule Technologie Sas - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2015

Total

Cleared

Denied

Capsule Technologie Sas has 4 FDA 510(k) cleared medical devices. Based in Andover, US.

Last cleared in 2021. Active since 2015. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Capsule Technologie Sas Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

Capsule Technologie Sas is one of 16345 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Capsule Technologie Sas

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 23, 2026