FDA applicant

Whiteside Instruments

Creve Coeur, MO1 decision1996–19961 recall

FDA records 1 decision for Whiteside Instruments (Creve Coeur, MO) in 1996: 1 510(k) clearance. All are in product code LPH (Prosthesis, Hip, Semi-Constrained…). 1 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 Whiteside Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Whiteside Instruments since 2007.

Recalls per year

1in 2014

2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Whiteside”

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

Whiteside Biomechanics, Inc. 13

Whiteside Instruments

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Whiteside”