510(k) Report

FDA applicant

U.S. Medical Instruments, Inc.

La Jolla, CA2 decisions1991–19940 recalls

FDA records 2 decisions for U.S. Medical Instruments, Inc. (La Jolla, CA) from 1991 to 1994: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and MEG (Syringe, Antistick). 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 U.S. Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for U.S. Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — U.S. Medical Instruments, 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?

  • FMFSyringe, Piston1decision
  • MEGSyringe, Antistick1decision

Who builds on its devices?

Later devices cite its devices 5 times; 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.

  • K925039Safesnap Safety SyringeU.S. Medical Instruments, Inc. · 19944cite it
  • K910520Safetysnap Safety SyringeU.S. Medical Instruments, Inc. · 19911cites it

What has FDA decided for it lately?

  • K925039Safesnap Safety SyringeU.S. Medical Instruments, Inc. · 1994
  • K910520Safetysnap Safety SyringeU.S. Medical Instruments, Inc. · 1991

All 2 as U.S. Medical Instruments, Inc. →