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 14, 2026, FDA's public records list Stimulation Technology, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 3, 1979: STIMTECH NEUROMUSCULAR STIMULATOR, C 600.
| Jul 3, 1979 | STIMTECH NEUROMUSCULAR STIMULATOR, C 600K791048 · IPF | 510(k) clearances |
| Mar 21, 1979 | STIMTECH TENS ELECTRODEK790345 · GXY | 510(k) clearances |
| Oct 11, 1978 | ELECTRICAL NERVE STIMULATOR MODEL 6035K781565 · GZJ | 510(k) clearances |
| Dec 15, 1977 | NERVE STIMULATOR, ELEC. TRANSCUTANEOUSK772224 · GZJ | 510(k) clearances |
| Mar 15, 1977 | EPC INSTICKSK770447 · GXY | 510(k) clearances |
| Mar 15, 1977 | INS - T.E.N.S.K770448 · GXY | 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
