FDA applicant

Mastek, Inc.

Houston, TX1 decision1999–19990 recalls

FDA records 1 decision for Mastek, Inc. (Houston, TX) in 1999: 1 510(k) clearance. All are in product code IXA (Cassette, Radiographic Film). 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 Mastek, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mastek, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mastek, Inc.

Which product codes does it file in?

What has FDA decided for it lately?