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 Kinetic Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 30, 1992: KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1.
| Date | Record | Source |
|---|---|---|
| Sep 30, 1992 | KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1K922693 · LXM | 510(k) clearances |
| Sep 30, 1992 | KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5K922695 · LXM | 510(k) clearances |
| Sep 30, 1992 | KINETIC TECHNOLOGY POCKET PRECISION ADJUSTORK922692 · LXM | 510(k) clearances |
| Sep 30, 1992 | KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4K922694 · LXM | 510(k) clearances |
| Apr 26, 1988 | PRECISION SPINAL ADJUSTER MODEL 115K870910 · LXM | 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
