Medical Device Manufacturer · JP , Shinjuku-Ku

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

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Reprolife, Inc. has 1 FDA 510(k) cleared medical devices. Based in Shinjuku-Ku, JP.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Obstetrics & Gynecology.

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

Reprolife, Inc. is one of 63 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.

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

1 devices

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