Medical Device Manufacturer · US , Shelton , CT

Mini Lap Technologies, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Mini Lap Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Shelton, US.

Historical record: 5 cleared submissions from 2007 to 2010. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Mini Lap Technologies, Inc. Filter by specialty or product code using the sidebar.

Mini Lap Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mini Lap Technologies, Inc.

5 devices

1-5 of 5