Medin Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medin Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medin Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1977 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medin Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medin Corp.
5 devices
Cleared
Jul 02, 1993
HARGIS SR2 SELF-RETRACTION SYSTEM
General & Plastic Surgery
486d
Cleared
Jul 02, 1993
HARGIS RECTAL SELF RETRATION SYSTEM
General & Plastic Surgery
486d
Cleared
Jul 02, 1993
HARGIS SELF RETRACTION SYSTEM
General & Plastic Surgery
486d
Cleared
Nov 03, 1983
STERILIZATION CONTAINER
General Hospital
37d
Cleared
Jan 26, 1977
CRADLING SYSTEM
General Hospital
72d