FDA applicant

Med Labs, Inc.

Goleta, CA4 decisions1990–19960 recalls

FDA records 4 decisions for Med Labs, Inc. (Goleta, CA) from 1990 to 1996: 4 510(k) clearances. Most are in product codes ILQ (System, Communication, Powered) and IPF (Stimulator, Muscle, 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Med Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Med Labs, 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?