Lexington International, LLC - FDA 510(k) Cleared Devices

Lexington International, LLC has 8 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 8 cleared submissions from 2007 to 2018. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Olsson Frank Weeda Terman Matz PC and Nst Consulting, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.