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 15, 2026, FDA's public records list Electro Therapeutic Devices, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 1998: ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES.
| Aug 24, 1998 | ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLESK981272 · MQX | 510(k) clearances |
| Sep 8, 1989 | ELECTRICAL MUSCLE STIMULATOR MODEL MYOAIDK875317 · IPF | 510(k) clearances |
| Oct 24, 1986 | 'TENSAID'K863567 · GZJ | 510(k) clearances |
| Oct 24, 1986 | 'MYOSTIM EX'K863568 · GZJ | 510(k) clearances |
| Dec 4, 1985 | TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 804K853718 · GZJ | 510(k) clearances |
| Dec 4, 1985 | TRANSCUTANEOUS ELECT. NERVE STIMUL-MYOSTIM 410K853719 · GZJ | 510(k) clearances |
| Aug 17, 1984 | ETI TENS BELTK843119 · GZJ | 510(k) clearances |
| Jul 14, 1977 | THERATHERMK770686 · IRT | 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
