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 Staodyne with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 4, 1995: VARAPULSE-2.
| Date | Record | Source |
|---|---|---|
| Dec 4, 1995 | VARAPULSE-2K952680 · IPF | 510(k) clearances |
| Jun 2, 1995 | STERILE TREATMENT ELECTRODEK941923 · GZJ | 510(k) clearances |
| Aug 16, 1993 | TPK CUTANEOUS ELECTRODEK931925 · GXY | 510(k) clearances |
| Aug 11, 1993 | STAODYN EMS+2K926510 · IPF | 510(k) clearances |
| Jun 4, 1993 | MAXIMA IK931424 · GZJ | 510(k) clearances |
| May 13, 1993 | STAODYN MAXIMA IIIK930865 · GZJ | 510(k) clearances |
| Jan 28, 1993 | MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUSK925898 · GZJ | 510(k) clearances |
| Aug 14, 1992 | TENSK921110 · GZJ | 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
