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 Dio-Med Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 1994: DIOMED 25 25W SURGICAL DIODE LASER.
| Date | Record | Source |
|---|---|---|
| Mar 1, 1994 | DIOMED 25 25W SURGICAL DIODE LASERK933525 · GEX | 510(k) clearances |
| Oct 19, 1993 | DIOMED 25 25W SURGICAL DIODE LASERK931776 · GEX | 510(k) clearances |
| Sep 23, 1993 | DIOMED 25 25W SURGICAL DIODE LASERK931212 · GEX | 510(k) clearances |
| Sep 16, 1993 | DIOMED 25 SURGICAL DIODE LASER, GYNECOLOGY APPLICK914519 · GEX | 510(k) clearances |
| Jan 22, 1993 | DIOMED 25 SURGICAL DIODE LASER, UROLOGY APPLICATK914520 · GEX | 510(k) clearances |
| Jan 15, 1993 | DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICATK914521 · GEX | 510(k) clearances |
| Dec 14, 1981 | DISPOSABLE DIAPHRAGM DOMESK813267 · DRS | 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
