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Corin USA

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
57
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K203751OMNIVision systemApril 12, 2021
K202805Optimized Positioning System (OPS) InsightNovember 20, 2020
K193545Corin Optimized Positioning System (OPS) FemoralAugust 4, 2020
K193042Optimized Positioning System (OPS) ReViewJune 26, 2020
K192656Optimized Positioning System (OPS) InsightMay 1, 2020
K190143LARS AC Band DeviceNovember 4, 2019
K190834Corin Optimized Position System Functional Hip Analysis (OPS FHA)July 22, 2019
K183038Corin Optimized Positioning System (OPS) PlanNovember 26, 2018
K181061Corin Optimized Positioning System (OPS) FemoralSeptember 7, 2018
K152893Corin Optimized Positioning System (OPS)June 3, 2016
K152903REVIVAL(TM) Modular Revision Hip StemApril 29, 2016
K142761Corin TaperFit Hip StemApril 3, 2015
K131986CORIN MINIHIP STEMDecember 16, 2013
K131952CORIN METAFIX HIP STEMDecember 16, 2013
K131647TRINITY ACETABULAR SYSTEMSeptember 27, 2013
K130343CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADSMay 28, 2013
K130634CORIN METAFIX HIP STEMMay 24, 2013
K123705TRINITY NON-OCCLUDED TITANIUM PLASMA SPRAYED (TPS) ACETABULAR SHELLSFebruary 12, 2013
K122305CORIN TRINITY-I ACETABULAR SHELLNovember 21, 2012
K121563CORIN TRIFIT TS HIPOctober 5, 2012