Koros USA, Inc. is one of 18943 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Koros USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DILATOR TUBE SET, SELF RETAINING SOFT TISSUE RETRACTOR, PECTUS STRUT
4
Total
4
Cleared
0
Denied
Koros USA, Inc. has 4 FDA 510(k) cleared medical devices. Based in Moorepark, US.
Historical record: 4 cleared submissions from 2007 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Koros USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Koros USA, Inc.
4 devices