Medical Device Manufacturer · US , Wausau , WI

Retrax - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Retrax has 1 FDA 510(k) cleared medical devices. Based in Wausau, US.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Gastroenterology & Urology.

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

Retrax 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 - Retrax

1 devices

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