Repromedix Corp. is one of 25870 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Repromedix Corp. - FDA 510(k) Cleared Devices
Recent clearances: REPROBEAD T4 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 105), REPROBEAD TSH ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 107), REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)
3
Total
3
Cleared
0
Denied
Repromedix Corp. has 3 FDA 510(k) cleared medical devices. Based in Woburn, US.
Historical record: 3 cleared submissions from 2000 to 2000. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Repromedix Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Repromedix Corp.
3 devices