FDA applicant

Mesa Medical, Inc.

Wheat Ridge, CO7 decisions1982–19940 recalls

FDA records 7 decisions for Mesa Medical, Inc. (Wheat Ridge, CO) from 1982 to 1994: 7 510(k) clearances. Most are in product codes LIF (Dialyzer Reprocessing System) and FLB (Meter, Conductivity, Induction, Remote Type). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Mesa Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mesa Medical, 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 “Mesa”

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

Mesa Laboratories, Inc. 9 Mesa Biotech, Inc. 3

Mesa Medical, 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 “Mesa”