FDA applicant

Automatic Medical Technologies, Inc.

Santa Ana, CA2 decisions2001–20030 recalls

FDA records 2 decisions for Automatic Medical Technologies, Inc. (Santa Ana, CA) from 2001 to 2003: 2 510(k) clearances. All are in product code LGZ (Warmer, Thermal, Infusion Fluid). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Automatic Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automatic Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Automatic Medical Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Automatic”

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

Automatic Liquid Packaging, Inc. 21 Automatic Film Processor Corp. 1

Automatic Medical Technologies, 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 “Automatic”