Medical Device Manufacturer · US , Buffalo Grove , IL

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

5 submissions · 5 cleared · Since 2002

Total

Cleared

Denied

Progeny, Inc. has 5 FDA 510(k) cleared medical devices. Based in Buffalo Grove, US.

Historical record: 5 cleared submissions from 2002 to 2009. Primary specialty: Radiology.

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

Progeny, Inc. is one of 21679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Progeny, Inc.

5 devices

1-5 of 5