FDA applicant

Orthopedic Source, Inc.

Loomis, CA3 decisions2001–20060 recalls

FDA records 3 decisions for Orthopedic Source, Inc. (Loomis, CA) from 2001 to 2006: 3 510(k) clearances. Most are in product codes LPH (Prosthesis, Hip, Semi-Constrained…) and JDI (Prosthesis, Hip, Semi-Constrained…). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 Orthopedic Source, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Orthopedic Source, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Orthopedic Source, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?