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FDA 510(k) Applications Submitted by Corin USA Limited
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231172
04/25/2023
ApolloKnee
Corin USA Limited
K153725
12/28/2015
Corin TaperFit Hip Stem
CORIN USA LIMITED
K153772
12/31/2015
Corin TriFit TS Hip
CORIN USA LIMITED
K183114
11/09/2018
Corin BiPolar-i
Corin USA Limited
K212069
07/02/2021
Corin MetaFixÖ Hip Stem
Corin USA Limited
K171847
06/21/2017
Corin Optimized Positioning System (OPSÖ) Plan
Corin USA Limited
K173884
12/21/2017
Unity Total Knee System
Corin USA Limited
K183533
12/19/2018
Unity Total Knee System
Corin USA Limited
K170808
03/17/2017
Unity Total Knee System
Corin USA Limited
K191374
05/23/2019
Revival Modular Hip Stem
Corin USA Limited
K172551
08/23/2017
Trinity PLUS Acetabular Shell
Corin USA Limited
K162942
10/21/2016
Corin MetaFix Hip Stem
CORIN USA LIMITED
K153381
11/23/2015
Corin Metafix Hip Stem
Corin USA Limited
K173880
12/21/2017
Corin TriFit CF Hip Stem
Corin USA Limited
K191831
07/09/2019
MobiliT Cup
Corin USA Limited
K170359
02/06/2017
TrinityÖ Dual Mobility System
Corin USA Limited
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