Reprolife, Inc. is one of 148 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
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.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Reprolife, Inc.
1 devices