Corin U.S.A. Limited
Corin U.S.A. Limited holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2025.
Top product codes for Corin U.S.A. Limited
Recent clearances by Corin U.S.A. Limited
- K242744 — Trinity EVO Acetabular Shell
- K241808 — ApolloHipX (THR.SS.0001)
- K241472 — Icona Hip Stem
- K241570 — Unity Total Knee System
- K240875 — Unity Knee PS-C Tibial Insert
- K231172 — ApolloKnee
- K212069 — Corin MetaFix Hip Stem
- K191831 — MobiliT Cup
- K191374 — Revival Modular Hip Stem
- K183114 — Corin BiPolar-i
- K183533 — Unity Total Knee System
- K172551 — Trinity PLUS Acetabular Shell
- K173880 — Corin TriFit CF Hip Stem
- K171847 — Corin Optimized Positioning System (OPS) Plan
- K173884 — Unity Total Knee System
- K170359 — Trinity Dual Mobility System
- K170808 — Unity Total Knee System
- K162942 — Corin MetaFix Hip Stem
- K153772 — Corin TriFit TS Hip
- K153725 — Corin TaperFit Hip Stem
- K153381 — Corin Metafix Hip Stem
Data sourced from openFDA. This site is unofficial and independent of the FDA.