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

Corin Orthopedic Products · Predicate Candidate Screening

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

376 daysmedian FDA review time
547 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K931752CORIN AUSTIN-MOORE PROSTHESIS, MODIFICATIONCorin Orthopedic Products1994-10-075470
K931753CORIN THOMPSON PROSTHESIS, MODIFICATIONCorin Orthopedic Products1994-10-075470
K934166NUFFIELD TOTAL KNEE UHMWPE TIBIA (ONE PIECE) MODIFICATIONCorin Orthopedic Products1994-09-073760
K925866CENATOR TOTAL HIP SYSTEMCorin Orthopedic Products1993-09-233080
K925897CORIN BIPOLAR PROSTHESISCorin Orthopedic Products1993-08-092630

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