FDA applicant

Automata Instrumentation, Inc.

Scottsdale, AZ3 decisions1997–19990 recalls

FDA records 3 decisions for Automata Instrumentation, Inc. (Scottsdale, AZ) from 1997 to 1999: 3 510(k) clearances. Most are in product codes FIZ (Meter, Conductivity, Non-Remote) and FIP (Subsystem, Water Purification). 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 Automata Instrumentation, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automata Instrumentation, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Automata Instrumentation, 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 “Automata”

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

Automata Medical Instrumentation, Inc. 2 Automata, Inc. 2

Automata Instrumentation, 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 “Automata”