FDA applicant

Meddev International Corp.

Los Altos, CA4 decisions1977–19940 recalls

FDA records 4 decisions for Meddev International Corp. (Los Altos, CA) from 1977 to 1994: 4 510(k) clearances. Most are in product codes KZF (Device, Medical Examination, Ac Powered) and KNX (Collector, Urine, (And Accessories) For…). 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, general hospital panel, where it files most

How often FDA has decided Meddev International Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Meddev International Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Meddev International Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Meddev”

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

Meddev Corp. 3

Meddev International Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Meddev”