Medical Device Manufacturer · US , Apollo Beach , FL

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

4 submissions · 4 cleared · Since 2005

Recent clearances: WELL LEAD SILICONE AND LATEX FOLEY CATHETERS, WELL LEAD REINFORCED ENDOTRACHEAL TUBE, WELL LEAD ENDOTRACHEAL TUBE

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

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

3 devices

1-3 of 3

Cleared Jul 10, 2008

WELL LEAD REINFORCED ENDOTRACHEAL TUBE

Anesthesiology · 220d

Cleared Feb 18, 2005

WELL LEAD ENDOTRACHEAL TUBE

Anesthesiology · 142d

Cleared Feb 17, 2005

WELL LEAD TRACHEOSTOMY TUBE

Anesthesiology · 141d

Data Source

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

Last updated: Sep 25, 2026