Medical Device Manufacturer · US , Irvine , CA

Rouge Ent., Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

Total

Cleared

Denied

Rouge Ent., Inc. has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

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

Rouge Ent., 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 - Rouge Ent., Inc.

1 devices

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