Medical Device Manufacturer · DE , Wittlingen

Lauer Ltd., Hong Kong - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: AQUABOSS ECORO DIA 50

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lauer Ltd., Hong Kong Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Oct 02, 2003

AQUABOSS ECORO DIA 50

Gastroenterology & Urology · 94d

Data Source

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

Last updated: Oct 11, 2026