FDA applicant

Adler Instrument Co.

Norcross, GA8 decisions1983–19910 recalls

FDA records 8 decisions for Adler Instrument Co. (Norcross, GA) from 1983 to 1991: 8 510(k) clearances. Most are in product codes HES (Insufflator, Carbon-Dioxide, Uterotubal (And…) and GAZ (Tubing, Noninvasive). 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 Adler Instrument Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Adler Instrument Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Adler Instrument Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Adler”

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

Adler Industries, Inc. 1 Adler Ortho S.P.A 1 Adler Micromed, Inc. 1

Adler Instrument Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Adler”