Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Euromed with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 28, 2008: SURESKIN SILVER BANDAGES.
| May 28, 2008 | SURESKIN SILVER BANDAGESK081274 · FRO | 510(k) clearances |
| May 17, 2006 | EUROMED SURESKIN III WITH SILVER WOUND DRESSINGSK050032 · FRO | 510(k) clearances |
| Aug 12, 1999 | SURESKIN II STANDARD, SURESKIN II BORDER, SURESKIN II THINK992363 · FRO | 510(k) clearances |
| Nov 25, 1998 | SURESKIN PLUS STANDARD, SURESKIN PLUS BORDER, SURESKIN PLUS THINK983249 · FRO | 510(k) clearances |
| Sep 23, 1996 | SURESKIN STANDARD, BORDER, AND THINK963039 · FRO | 510(k) clearances |
| Mar 1, 1996 | SURESKIN BORDERK960393 · MGP | 510(k) clearances |
| Mar 1, 1996 | SURESKIN STANDARDK960394 · MGP | 510(k) clearances |
| Mar 1, 1996 | SURESKIN THINK960404 · MGP | 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
