Medical Device Manufacturer · US , Mchenry , IL

Cintor Orthopaedic Div. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1980

Total

Cleared

Denied

Cintor Orthopaedic Div. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1980 to 1981. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Cintor Orthopaedic Div.

7 devices

1-7 of 7