Reprobitech Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reprobitech Corp. - FDA 510(k) Cleared Devices
Recent clearances: iVitri Straw
2
Total
2
Cleared
0
Denied
Reprobitech Corp. has 2 FDA 510(k) cleared medical devices. Based in New Hyde Park, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Reprobitech Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reprobitech Corp.
2 devices