FDA applicant

Imt America, Inc.

Baltimore, MD5 decisions1990–19900 recalls

FDA records 5 decisions for Imt America, Inc. (Baltimore, MD) in 1990: 5 510(k) clearances. Most are in product codes IXR (Table, Radiographic, Tilting) and OXO (Image-Intensified Fluoroscopic X-Ray System…). 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 Imt America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Imt America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Imt America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?