FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Dymax Corporation with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jul 21, 2003: SITE-RITE IV ULTRASOUND SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jul 21, 2003 | SITE-RITE IV ULTRASOUND SYSTEMK032135 · IYO | 510(k) clearances |
| Nov 10, 1999 | SITE-RITE 3 ULTRASOUND SYSTEMK993624 · IYO | 510(k) clearances |
| Jul 27, 1993 | SITERITE NEEDLE GUIDE (MODIFIED)K931403 · DQY | 510(k) clearances |
| Sep 27, 1990 | SITERITE NEEDLE GUIDEK903158 · DQY | 510(k) clearances |
| Oct 25, 1989 | DYMAX ENDOVAGINAL BIOPSY GUIDEK894415 · HGL | 510(k) clearances |
| Dec 11, 1986 | DYMAX PERSONAL SCANNERK862127 · IYO | 510(k) clearances |
| Apr 15, 1985 | PLUS 1K850478 · IYO | 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
