Corin U.S.A. Limited

FDA Regulatory Profile

Corin U.S.A. Limited appears in FDA public data with 0 recalls, 21 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 5, 2025.

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Known Names

Corin Usa Limited, Corin U.S.A. Limited

Recent 510(k) Clearances

K-NumberDeviceDate
K242744Trinity EVO Acetabular ShellJun 5, 2025
K241808ApolloHipX (THR.SS.0001)Jan 7, 2025
K241472Icona Hip StemOct 3, 2024
K241570Unity Total Knee SystemSep 23, 2024
K240875Unity Knee PS-C Tibial InsertJun 26, 2024
K231172ApolloKneeJul 26, 2023
K212069Corin MetaFix™ Hip StemApr 7, 2022
K191831MobiliT CupJan 16, 2020
K191374Revival Modular Hip StemJul 22, 2019
K183114Corin BiPolar-iJun 5, 2019
K183533Unity Total Knee SystemJun 4, 2019
K172551Trinity PLUS Acetabular ShellJun 15, 2018
K173880Corin TriFit CF Hip StemApr 11, 2018
K171847Corin Optimized Positioning System (OPS™) PlanApr 5, 2018
K173884Unity Total Knee SystemJan 17, 2018
K170359Trinity™ Dual Mobility SystemOct 31, 2017
K170808Unity Total Knee SystemJul 13, 2017
K162942Corin MetaFix Hip StemJun 20, 2017
K153772Corin TriFit TS HipMar 31, 2016
K153725Corin TaperFit Hip StemMar 25, 2016