Rejoni, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rejoni, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rejoni Intrauterine Catheter
1
Total
1
Cleared
0
Denied
Rejoni, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bedford, US.
Last cleared in 2022. Active since 2022. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Rejoni, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rejoni, Inc.
1 devices