Medical Device Manufacturer · CA , Canada Law1v6

Manexim Multicorp, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1985

Total

Cleared

Denied

Manexim Multicorp, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Canada Law1v6, CA.

Historical record: 5 cleared submissions from 1985 to 1986. Primary specialty: Obstetrics & Gynecology.

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

Manexim Multicorp, Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Manexim Multicorp, Ltd.

5 devices

1-5 of 5