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 14, 2026, FDA's public records list Medical Concepts Development with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 18, 2002: COLOSHIELD COLONOSCOPY DRAPE MODEL E2000.
| Sep 18, 2002 | COLOSHIELD COLONOSCOPY DRAPE MODEL E2000K020581 · KKX | 510(k) clearances |
| Apr 24, 2001 | ACTI-GARD ANTIMICROBIAL FILM, MODELS D6635, D6640, D6648, D6650,D6651, D66XXK000442 · KKX | 510(k) clearances |
| Jul 8, 1993 | TRANSPARENT ADHESIVE DRESSINGK924794 · KGX | 510(k) clearances |
| Jan 21, 1987 | MCD SPECIALTY BRAND NEEDLE COUNTERSK870044 · | 510(k) clearances |
| May 30, 1986 | SURGICAL PACKS, KITS AND TRAYSK861530 · FSM | 510(k) clearances |
| May 23, 1986 | DISPOSABLE SURGICAL DRAPES AND ACCESSORIESK861531 · KKX | 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
