Medical Device Manufacturer · US , Mchenry , IL

Ultralite - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1977

Total

Cleared

Denied

Ultralite has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1977 to 1991. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Ultralite

6 devices

1-6 of 6