Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Staodynamics with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 1985: TENS-AID STERILE ELECTRODES FOR POST-OP TENS.
| Date | Record | Source |
|---|---|---|
| Jun 24, 1985 | TENS-AID STERILE ELECTRODES FOR POST-OP TENSK852298 · GXY | 510(k) clearances |
| Feb 25, 1985 | TENS-AID PREMIUM ELECTRODESK843964 · GXY | 510(k) clearances |
| Nov 22, 1983 | STAODYN EMS/PLUSK832988 · IPF | 510(k) clearances |
| Feb 10, 1982 | 10D (TENS DEVICE)K813283 · GZJ | 510(k) clearances |
| Nov 20, 1981 | TENS DEVICEK813098 · | 510(k) clearances |
| Jul 10, 1981 | INSIGHTK811345 · GZJ | 510(k) clearances |
| Feb 26, 1980 | POINT LOCATOR STIMULATORK792529 · BWJ | 510(k) clearances |
| Feb 26, 1980 | PLS MINIK792501 · BWJ | 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
