Medical device makerLabelled 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., part of Becton, Dickinson and CompanyLabelled 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 14, 2026, FDA's public records list Cormed with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 1986: BUTTERFLY NON-CORING NEEDLE SET.
| Dec 18, 1986 | BUTTERFLY NON-CORING NEEDLE SETK863606 · FMI | 510(k) clearances |
| Mar 31, 1986 | PERCUTANEOUS INTRODUCER KITK860432 · DYB | 510(k) clearances |
| Nov 26, 1985 | PORT-GARDK854019 · LJT | 510(k) clearances |
| May 17, 1985 | STERILE CORMED MEDIPORTK850967 · LJT | 510(k) clearances |
| Apr 9, 1985 | CORMED II AMBULATORY INFUSION PUMPK850674 · FRN | 510(k) clearances |
| Sep 5, 1984 | CORMED HUBER POINT NEEDLEK843083 · GAA | 510(k) clearances |
| Mar 30, 1984 | VASCULAR ACCESS CATH. REPAIR KITK833915 · LJS | 510(k) clearances |
| Jan 5, 1983 | CORCATH H & B VASCULAR ACCESS CATHETERK823553 · LJS | 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
