FDA applicant

Medix Biotech, Inc.

Foster City, CA39 decisions1985–19950 recalls

FDA records 39 decisions for Medix Biotech, Inc. (Foster City, CA) from 1985 to 1995: 39 510(k) clearances. Most are in product codes JHI (Visual, Pregnancy Hcg, Prescription Use) and CGJ (Radioimmunoassay, Follicle-Stimulating Hormone). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Medix Biotech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medix Biotech, 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 “Medix”

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

Medix Medical Electronics (U.S.A.), Inc. 14 Medix I.C.S.A. 6 Medix Corp. 6 Medix Biochemica 1 Medix of Florida, Inc. 1 Medix Pharmaceuticals Americas, Inc. 1

Medix Biotech, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medix”