FDA applicant

Orthopaedic Device Corp.

Allendale, NJ4 decisions1986–19870 recalls

FDA records 4 decisions for Orthopaedic Device Corp. (Allendale, NJ) from 1986 to 1987: 4 510(k) clearances. Most are in product codes KWY (Prosthesis, Hip, Hemi-, Femoral…) and KWL (Prosthesis, Hip, Hemi-, Femoral, Metal). 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 Orthopaedic Device Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Orthopaedic Device Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Orthopaedic Device Corp.

Which product codes does it file in?

What has FDA decided for it lately?