510(k) Report

FDA applicant

Modern Medical Devices, Inc.

Fremont, CA1 decision1994–19940 recalls

FDA records 1 decision for Modern Medical Devices, Inc. (Fremont, CA) in 1994: 1 510(k) clearance. All are in product code BZS (Stethoscope Head). 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, anesthesiology panel, where it files most

How often FDA has decided Modern Medical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Modern Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Modern Medical Devices, Inc.’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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Other applicant names beginning “Modern”

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