Well Lead Medical Co., Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Well Lead Medical Co., Ltd. has 17 FDA 510(k) cleared gastroenterology & urology devices. Based in Apollo Beach, US.
Latest FDA clearance: Mar 2025. Active since 2009.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Well Lead Medical Co., Ltd.
17 devices
Cleared
Mar 05, 2025
Wellead® Hydrophilic Intermittent Catheter Ready to Use
Gastroenterology & Urology
261d
Cleared
May 22, 2023
PVC Hydrophilic Urethral Catheter
Gastroenterology & Urology
434d
Cleared
Dec 16, 2022
Wellead Ureteral Catheter
Gastroenterology & Urology
345d
Cleared
Jul 21, 2022
Wei Nasal Jet Tube
Anesthesiology
428d
Cleared
Jan 14, 2022
Wellead Endoscopic Seal
Gastroenterology & Urology
217d
Cleared
Apr 08, 2021
Well Lead All Silicone Foley Catheter with Temperature Sensor
Gastroenterology & Urology
251d
Cleared
Dec 09, 2020
ClearPetra Suction-Evacuation Sheath
Gastroenterology & Urology
54d
Cleared
Dec 11, 2019
Endotracheal Tube with Evacuation Lumen
Anesthesiology
439d
Cleared
Oct 11, 2017
Stomach Tube
Gastroenterology & Urology
415d
Cleared
Nov 29, 2016
Well Lead Extraction Bag
General & Plastic Surgery
251d
Cleared
Oct 12, 2016
ClearPetra Suction-Evacuation Sheath
Gastroenterology & Urology
175d
Cleared
Jan 07, 2016
Well Lead Ureteral Access Sheath
Gastroenterology & Urology
260d