Medical Device Manufacturer · US , Mchenry , IL

Dio-Med Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1981

Total

Cleared

Denied

Dio-Med Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1981 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Dio-Med Corp. Filter by specialty or product code using the sidebar.

Dio-Med Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dio-Med Corp.

7 devices

1-7 of 7