510(k) Report

FDA applicant

International Medical Device Partners, Inc.

Los Angeles, CA1 decision2001–20010 recalls

FDA records 1 decision for International Medical Device Partners, Inc. (Los Angeles, CA) in 2001: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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 hospital panel, where it files most

How often FDA has decided International Medical Device Partners, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for International Medical Device Partners, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K003406Guarded Needle 2000International Medical Device Partners, Inc. · 20011cites it

What has FDA decided for it lately?

  • K003406Guarded Needle 2000International Medical Device Partners, Inc. · 2001

The one decision as International Medical Device Partners, Inc. →