FDA applicant

Magna Fortis Corporation

Bellevue, WA1 decision2000–20000 recalls

FDA records 1 decision for Magna Fortis Corporation (Bellevue, WA) in 2000: 1 510(k) clearance. All are in product code HLJ (Ophthalmoscope, Battery-Powered). 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, ophthalmic panel, where it files most

How often FDA has decided Magna Fortis Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magna Fortis Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magna Fortis Corporation 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 Advanced Technologies, Inc. 7 Magna-Lab, Inc. 4 Magna Intl., Inc. 1

Magna Fortis Corporation

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Magna”