FDA applicant
Control-X, Inc.
FDA records 9 decisions for Control-X, Inc. (Columbus, OH) from 1991 to 1995: 9 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and 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
How often FDA has decided Control-X, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Control-X, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Control-X, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Control-X”
FDA records each applicant name separately; these may or may not be the same firm.