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.

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

5 devices

1-5 of 5