FDA applicant

Magna Advanced Technologies, Inc.

Miami, FL7 decisions1998–19990 recalls

FDA records 7 decisions for Magna Advanced Technologies, Inc. (Miami, FL) from 1998 to 1999: 7 510(k) clearances. Most are in product codes DQA (Oximeter) and CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). 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 Magna Advanced Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magna Advanced Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magna Advanced Technologies, 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 “Magna”

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

Magna-Lab, Inc. 4 Magna Fortis Corporation 1 Magna Intl., Inc. 1

Magna Advanced Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Magna”