Medical Device Manufacturer · US , Mchenry , IL

I-Rep, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1982

Total

Cleared

Denied

I-Rep, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1982 to 1994. Primary specialty: Physical Medicine.

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

I-Rep, 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 - I-Rep, Inc.

8 devices

1-8 of 8