510(k) Report

FDA applicant

Danninger Medical Technology, Inc.

Concord, CA6 decisions1984–19940 recalls

FDA records 6 decisions for Danninger Medical Technology, Inc. (Concord, CA) from 1984 to 1994: 6 510(k) clearances. Most are in product codes BXB (Exerciser, Powered) and HWJ (Awl). 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, physical medicine panel, where it files most

How often FDA has decided Danninger Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Danninger Medical Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Danninger Medical Technology, 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?

  • BXBExerciser, Powered3decisions
  • HWJAwl1decision
  • ILOPack, Hot Or Cold, Water Circulating1decision
  • JFAExerciser, Finger, Powered1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K913026Ttu-100THERMAL Therapy UnitDanninger Medical Technology, Inc. · 19911cites it

What has FDA decided for it lately?

  • K931128Basic Shoulder CPMDanninger Medical Technology, Inc. · 1994
  • K933394Danniflex CPM 600Danninger Medical Technology, Inc. · 1994
  • K913026Ttu-100THERMAL Therapy UnitDanninger Medical Technology, Inc. · 1991
  • K875223Danninger Orthopaedic AwlDanninger Medical Technology, Inc. · 1988
  • K862730Danniflex 400SLDanninger Medical Technology, Inc. · 1986
  • K844033Mobilimb Hand UnitDanninger Medical Technology, Inc. · 1984

All 6 as Danninger Medical Technology, Inc. →