Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Corin USA — Predicate Candidate Screening

57 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

110 daysmedian FDA review time

268 days90th percentile

57clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K203751	OMNIVision system	Corin USA	2021-04-12	110	0
K202805	Optimized Positioning System (OPS) Insight	Corin USA	2020-11-20	58	0
K193545	Corin Optimized Positioning System (OPS) Femoral	Corin USA	2020-08-04	228	0
K193042	Optimized Positioning System (OPS) ReView	Corin USA	2020-06-26	239	0
K192656	Optimized Positioning System (OPS) Insight	Corin USA	2020-05-01	219	0
K190143	LARS AC Band Device	Corin USA	2019-11-04	279	0
K190834	Corin Optimized Position System Functional Hip Analysis (OPS	Corin USA	2019-07-22	112	0
K183038	Corin Optimized Positioning System (OPS) Plan	Corin USA	2018-11-26	25	0
K181061	Corin Optimized Positioning System (OPS) Femoral	Corin USA	2018-09-07	137	0
K152893	Corin Optimized Positioning System (OPS)	Corin USA	2016-06-03	247	0
K152903	REVIVAL(TM) Modular Revision Hip Stem	Corin USA	2016-04-29	211	0
K142761	Corin TaperFit Hip Stem	Corin USA	2015-04-03	190	0
K131986	CORIN MINIHIP STEM	Corin USA	2013-12-16	171	0
K131952	CORIN METAFIX HIP STEM	Corin USA	2013-12-16	172	0
K131647	TRINITY ACETABULAR SYSTEM	Corin USA	2013-09-27	114	0
K130343	CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS	Corin USA	2013-05-28	106	0
K130634	CORIN METAFIX HIP STEM	Corin USA	2013-05-24	74	0
K123705	TRINITY NON-OCCLUDED TITANIUM PLASMA SPRAYED (TPS) ACETABULA	Corin USA	2013-02-12	71	0
K122305	CORIN TRINITY-I ACETABULAR SHELL	Corin USA	2012-11-21	112	0
K121563	CORIN TRIFIT TS HIP	Corin USA	2012-10-05	129	0
K121439	METAFIX FEMORAL HIP STEM SIZE 1	Corin USA	2012-09-14	122	0
K113060	UNITY TOATAL KNEE SYSTEM	Corin USA	2012-09-10	332	3
K120362	METAFIX FEMORAL STEM FOR HEMI-ARTHROPLASTY	Corin USA	2012-05-04	88	0
K111481	CORIN TRINITY ACETABULAR SYSTEM ECIMA LINERS	Corin USA	2012-02-06	255	0
K111911	CORIN OPTIMOM MODULAR HEAD	Corin USA	2011-08-04	30	0
K111046	CORIN MINIHIP FEMORAL STEM	Corin USA	2011-06-29	75	0
K110087	CORIN TRINITY ACETBULAR SYSTEM WITH HXLPE LINERS	Corin USA	2011-05-03	111	0
K103518	TRINITY ACETABULAR SYSTEM	Corin USA	2011-03-09	99	0
K103120	CORIN BIOLOX DELTA FEMORAL HEADS	Corin USA	2011-02-28	129	0
K093472	TRINITY ACETABULAR SYSTEM	Corin USA	2010-11-23	382	0
K092198	CORMET CEMENTLESS RESURFACING FEMORAL HEAD	Corin USA	2010-04-15	268	0
K083312	MINIHIP STEM	Corin USA	2010-04-05	511	0
K082525	CORIN METAFIX FEMORAL STEM	Corin USA	2010-02-04	520	0
K063791	CORIN UNIPOLAR MODULAR HEAD	Corin USA	2007-04-03	102	0
K050764	UNIGLIDE UNICONDYLAR KNEE PROSTHESIS	Corin USA	2005-08-24	153	0
K022798	CERVIVE ANTERIOR CERVICAL PLATING SYSTEM, MODEL NUMBER 157.X	Corin USA	2002-11-19	88	0
K012377	OXFORD MODULAR SHOULDER PROSTHESIS, 192.XXX CATALOGUE SERIES	Corin USA	2002-03-11	228	0
K010776	TRINITY POLYAXIAL SCREW, MEHDIAN SPINAL ROD (6MM), MODEL 159	Corin USA	2001-04-06	23	0
K010243	TRI-FIT FEMORAL STEM	Corin USA	2001-02-15	21	0
K003666	TAPER-FIT TOTAL HIP SYSTEM	Corin USA	2001-02-08	72	0
K000634	ROD TO ROD CROSS BRACES	Corin USA	2000-03-10	14	0
K994152	THE LIGAMENT ANCHOR SOFT SCREW	Corin USA	2000-03-06	89	0
K000232	ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS	Corin USA	2000-02-25	29	0
K994153	CORMET 2000 HEMI HIP METALLIC RESURFACING PROSTHESIS	Corin USA	2000-02-25	79	0
K992235	ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS	Corin USA	1999-11-23	144	0
K992234	THE TAPER-FIT TOTAL HIP SYSTEM	Corin USA	1999-11-10	131	0
K990657	TRIFIX PEDICLE SPINAL SCREW ASSEMBLY	Corin USA	1999-03-26	25	0
K980545	THE NUFFIELD TOTAL KNEE SYSTEM	Corin USA	1998-04-29	76	0
K973425	THE MEHDIAN LUMBO-SACRAL PEDICLE SCREW SYSTEM	Corin USA	1998-02-27	170	0
K973595	THE POSTERIOR STABILISED NUFFIELD TOTAL KNEE SYSTEM	Corin USA	1997-12-19	88	0

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda