Curatia Medical Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curatia Medical Co. - FDA 510(k) Cleared Devices
Recent clearances: EXTesia Introducer Sheath Set, Xcess Guiding Catheter
2
Total
2
Cleared
0
Denied
Curatia Medical Co. has 2 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Last cleared in 2022. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Curatia Medical Co. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Jcq Consulting and Prime Path Medtech.
FDA 510(k) Regulatory Record - Curatia Medical Co.
2 devices