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 Editek with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 10, 1996: VERDICT PCP.
| Date | Record | Source |
|---|---|---|
| Dec 10, 1996 | VERDICT PCPK963692 · LCM | 510(k) clearances |
| Oct 31, 1996 | EZ-SCREEN PROFILEK963233 · LCM | 510(k) clearances |
| Oct 30, 1996 | VERDICT BARBITURATESK963529 · DIS | 510(k) clearances |
| Oct 30, 1996 | VERDICT THCK963516 · LDJ | 510(k) clearances |
| Nov 17, 1994 | VERDICT COCAINEK943710 · DIO | 510(k) clearances |
| Nov 17, 1994 | VERDICT OPIATESK943712 · DJG | 510(k) clearances |
| Sep 9, 1994 | EZ-SCREEN:PCPK943711 · LCM | 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
