FDA applicant

Absolute X-Ray Corp.

Long Island City, NY3 decisions1986–19880 recalls

FDA records 3 decisions for Absolute X-Ray Corp. (Long Island City, NY) from 1986 to 1988: 3 510(k) clearances. Most are in product codes ITY (Assembly, Tube Housing, X-Ray, Diagnostic) and IZO (Generator, High-Voltage, 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 Absolute X-Ray Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Absolute X-Ray Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Absolute”

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

Absolute Synthetic Technologies Malaysia Sdn. Bhd. 3 Absolute Quality Leadership, Inc. 1 Absolute Advantage Medical, LLC 1 Absolute Imaging Solutions 1

Absolute X-Ray Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Absolute”