Medical Device Manufacturer · US , Williston , VT

Laborie Medical Technologies, Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2008

Total

Cleared

Denied

Laborie Medical Technologies, Corp. has 5 FDA 510(k) cleared medical devices. Based in Williston, US.

Latest FDA clearance: Aug 2024. Active since 2008. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Laborie Medical Technologies, Corp. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Laborie Medical Technologies, Corp. is one of 16118 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Laborie Medical Technologies, Corp.

5 devices

1-5 of 5