Medical Device Manufacturer · US , Woodinville , WA

Lightscalpel, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

Lightscalpel, LLC has 5 FDA 510(k) cleared medical devices. Based in Woodinville, US.

Historical record: 5 cleared submissions from 2012 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Lightscalpel, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Lightscalpel, LLC

5 devices

1-5 of 5