Medical Device Manufacturer · US , Mchenry , IL

Visidyne Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1981

Total

Cleared

Denied

Visidyne Corp. has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 3 cleared submissions from 1981 to 1981. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Visidyne Corp.

3 devices

1-3 of 3