Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Dynatronics Corporation with 25 510(k) clearances. The most recent is a 510(k) clearance dated Jan 24, 2014: DYNATRON PELTIER THERMOSTIM PROBE.
| Jan 24, 2014 | DYNATRON PELTIER THERMOSTIM PROBEK132057 · GXY | 510(k) clearances |
| Aug 20, 2012 | DYNATRON THERMOSTIM PROBE-DONEK120835 · GXY | 510(k) clearances |
| Feb 9, 2012 | DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK113250 · ILY | 510(k) clearances |
| Jun 14, 2006 | DYNATRON ION IONTOPHORESIS ELECTRODEK060814 · EGJ | 510(k) clearances |
| Oct 11, 2005 | DYNATRON DX2 TRACTION UNITK051680 · ILY | 510(k) clearances |
| Jul 25, 2005 | DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEK051261 · ILY | 510(k) clearances |
| Jan 7, 2005 | DYNATRON IBOX IONTOPHORESIS DEVICEK043047 · EGJ | 510(k) clearances |
| Jun 2, 2004 | SOLARIS D890 THERAPY PROBEK040729 · ILY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
