510(k) Report

FDA applicant

Tingle X-Ray Products, Inc.

Vance, AL3 decisions1986–19930 recalls

FDA records 3 decisions for Tingle X-Ray Products, Inc. (Vance, AL) from 1986 to 1993: 3 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and IXY (Holder, Radiographic Cassette, Wall-Mounted). 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 Tingle X-Ray Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tingle X-Ray Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KPRSystem, X-Ray, Stationary1decision
  • IXYHolder, Radiographic Cassette, Wall-Mounted1decision
  • IZOGenerator, High-Voltage, X-Ray, Diagnostic1decision

What has FDA decided for it lately?

  • K926554525 SFQ X-Ray Control W/High Voltage GeneratorTingle X-Ray Products, Inc. · 1993
  • K930249BC/WT/PFTingle X-Ray Products, Inc. · 1993
  • K860203TXR 325 X-Ray Control with High Voltage GeneratorTingle X-Ray Products, Inc. · 1986

All 3 as Tingle X-Ray Products, Inc. →