Corin, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corin, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Corin Ltd. Hip Products: Trinity™ Acetabular System, Trinity™ PLUS Acetabular Shell, MetaFix™ Hip System, TriFit™ CF and TS Hip Systems, TaperFit™ Hip System, Revival™ Modular Hip System, MiniHip™, Trinity™ Dual Mobility, MobiliT, BiPolar-i, OMNI MOD™ Hip System, OMNI K1 and K2 Hip Systems, OMNI Bipolar Heads, Corin Biolox Delta Ceramic Heads, OMNI Delta Ceramic Heads, OMNIBotics Knee System
2
Total
2
Cleared
0
Denied
Corin, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Raynham, US.
Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Corin, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Corin, Ltd.
2 devices