FDA applicant

Dial-A-Rad

Orlando, FL1 decision1992–19920 recalls

FDA records 1 decision for Dial-A-Rad (Orlando, FL) in 1992: 1 510(k) clearance. All are in product code IXQ (Table, Radiographic, Stationary Top). 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 Dial-A-Rad’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dial-A-Rad since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dial-A-Rad’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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Other applicant names beginning “Dial-A-Rad”

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

Dial Medical of Florida, Inc. 2 Dial-X Instruments, Inc. 1 Dial Medical Supply 1

Dial-A-Rad

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dial-A-Rad”