FDA applicant

Multi Biosensors, Inc.

El Paso, TX2 decisions1985–19870 recalls

FDA records 2 decisions for Multi Biosensors, Inc. (El Paso, TX) from 1985 to 1987: 2 510(k) clearances. All are in product code DRX (Electrode, Electrocardiograph). 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, cardiovascular panel, where it files most

How often FDA has decided Multi Biosensors, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multi Biosensors, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Multi Biosensors, 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 “Multi”

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

Multi-Med, Inc. 8 Multi Radiance Medical 3 Multi M Intl., Inc. 2 Multi Trading Corp. of America, Inc. 1 Multi-Com Sdn Bhd 1 Multi-Dimensional Imaging, Inc. 1 Multi-Channel Epilator 1 Multi-Spectrum Consulting, Inc. 1 Multi-Wash Medical, Ltd. 1 Multi Media Dental Systems, Inc. 1

Multi Biosensors, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Multi”