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 J-Tech, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 3, 1996: SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE.
| Date | Record | Source |
|---|---|---|
| Jul 3, 1996 | SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICEK954737 · HCC | 510(k) clearances |
| Oct 30, 1995 | INCLINOMETERK954647 · KQX | 510(k) clearances |
| May 10, 1995 | LARGE MUSCLE STRENGTH GAUGEK945630 · KQX | 510(k) clearances |
| Oct 23, 1991 | JTECH 50 SERIES CUTTING LOOPK913587 · FJL | 510(k) clearances |
| Sep 5, 1991 | GS-220 HAND IMPAIRMENT EVALUATION SYSTEMK912526 · LBB | 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
