FDA applicant

Modern Engineering Co., Inc.

St. Louis, MO2 decisions1989–19890 recalls

FDA records 2 decisions for Modern Engineering Co., Inc. (St. Louis, MO) in 1989: 2 510(k) clearances. All are in product code CAN (Regulator, Pressure, Gas Cylinder). 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 Engineering Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Modern Engineering Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Modern”

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

Modern Medical Equipment Mfg., Ltd. 14 Modern Medical Equipment Manufacturing Limited 8 Modern Diagnostics, Inc. 5 Modern Rubber Industrial Co., Ltd. 5 Modern Healthcare Corp. 3 Modern Dental Laboratory (Dg) Co., Ltd. 2 Modern Materials 2 Modern Medical Systems Co. 2 Modern Systems Technology, Inc. 2 Modern Medical Devices, Inc. 1 Modern Rubber Co., Ltd. C/O World Trade Svc. 1 Modern Medical Products 1

Modern Engineering Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Modern”