510(k) Report

FDA applicant

Dan Kline

Carlsbad, CA1 decision1995–19950 recalls

FDA records 1 decision for Dan Kline (Carlsbad, CA) in 1995: 1 510(k) clearance. All are in product code LZW (Monitor, Spine Curvature). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Dan Kline’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dan Kline since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dan Kline 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?

  • LZWMonitor, Spine Curvature1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K951244Spine Tuner Posture TrainerDan Kline · 19952cite it

What has FDA decided for it lately?

  • K951244Spine Tuner Posture TrainerDan Kline · 1995

The one decision as Dan Kline →