FDA applicant

Inmark Corp.

Norwalk, CT4 decisions1989–19910 recalls

FDA records 4 decisions for Inmark Corp. (Norwalk, CT) from 1989 to 1991: 4 510(k) clearances. All are in product code ITY (Assembly, Tube Housing, X-Ray, 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, radiology panel, where it files most

How often FDA has decided Inmark Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inmark Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Inmark Corp.

Which product codes does it file in?

What has FDA decided for it lately?