510(k) Report

FDA applicant

Control-X Medical, Inc.

Columbus, OH1 decision2010–20100 recalls

FDA records 1 decision for Control-X Medical, Inc. (Columbus, OH) in 2010: 1 510(k) clearance. All are in product code KPR (System, X-Ray, Stationary). 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 Control-X Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Control-X Medical, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Control-X Medical, Inc.’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 “Control-X”

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