FDA applicant

Medical Device Resource Corp.

Hayward, CA2 decisions2008–20090 recalls

FDA records 2 decisions for Medical Device Resource Corp. (Hayward, CA) from 2008 to 2009: 2 510(k) clearances. Most are in product codes MUU (System, Suction, Lipoplasty) and QPB (System, Suction, Lipoplasty For Removal). Its devices cite 5 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, general and plastic surgery panel, where it files most

How often FDA has decided Medical Device Resource Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Medical Device Resource Corp. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medical Device Resource Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Medical Device Resource Corp.

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?