FDA applicant

Corin Orthopedic Products

Tampa, FL5 decisions1993–19940 recalls

FDA records 5 decisions for Corin Orthopedic Products (Tampa, FL) from 1993 to 1994: 5 510(k) clearances. Most are in product codes KWL (Prosthesis, Hip, Hemi-, Femoral, Metal) and JWH (Prosthesis, Knee, Patellofemorotibial…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Corin Orthopedic Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Corin Orthopedic Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Corin Orthopedic Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Corin”

FDA records each applicant name separately; these may or may not be the same firm.

Corin USA 79 Corin, Ltd. 4 Corin Medical 1

Corin Orthopedic Products

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Corin”