Medical Device Manufacturer · US , Mchenry , IL

Serrano Intl. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1981

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 1981 to 1985. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Serrano Intl.

6 devices

1-6 of 6