FDA applicant

Automata, Inc.

Scottsdale, AZ2 decisions1987–19880 recalls

FDA records 2 decisions for Automata, Inc. (Scottsdale, AZ) from 1987 to 1988: 2 510(k) clearances. All are in product code FIZ (Meter, Conductivity, Non-Remote). 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, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automata, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Automata, 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 Instrumentation, Inc. 3 Automata Medical Instrumentation, Inc. 2

Automata, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Automata”