Medical Device Manufacturer · US , Pine Brook , NJ

Diopsys, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Diopsys, Inc. has 2 FDA 510(k) cleared medical devices. Based in Pine Brook, US.

Historical record: 2 cleared submissions from 2005 to 2011. Primary specialty: Neurology.

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

Diopsys, Inc. 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 - Diopsys, Inc.

2 devices

1-2 of 2