Medical Device Manufacturer · US , Apollo Beach , FL

Well Lead Medical Instruments - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2005

Total

Cleared

Denied

Well Lead Medical Instruments has 4 FDA 510(k) cleared medical devices. Based in Apollo Beach, US.

Historical record: 4 cleared submissions from 2005 to 2008. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Well Lead Medical Instruments is one of 18354 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Well Lead Medical Instruments

4 devices

1-4 of 4

Data Source

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

Last updated: Sep 25, 2026