510(k) Report

FDA applicant

All-Pro Imaging Corp.

Hicksville, NY4 decisions1991–20000 recalls

FDA records 4 decisions for All-Pro Imaging Corp. (Hicksville, NY) from 1991 to 2000: 4 510(k) clearances. Most are in product codes IXW (Processor, Radiographic-Film, Automatic) and HEX (Colposcope (And Colpomicroscope)). 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 All-Pro Imaging Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for All-Pro Imaging Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like All-Pro Imaging Corp.’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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