FDA applicant

Aaron Laboratories, Inc.

San Antonio, TX2 decisions1988–19880 recalls

FDA records 2 decisions for Aaron Laboratories, Inc. (San Antonio, TX) in 1988: 2 510(k) clearances. All are in product code IKN (Electromyograph, Diagnostic). 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 Aaron Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aaron Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aaron Laboratories, 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 “Aaron”

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

Aaron Medical Industries 46 Aaron Medical, Inc. 3

Aaron Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Aaron”