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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Deroyal with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 2, 2004: EXAC-TEMP FOLEY CATHETER AND CLINI-TEMP FOLEY CATHETER.
| Jul 2, 2004 | EXAC-TEMP FOLEY CATHETER AND CLINI-TEMP FOLEY CATHETERK041416 · EYC | 510(k) clearances |
| Nov 20, 2003 | DEROYAL SURGICAL GOWNS, STERILE, NON-STERILEK033057 · FYA | 510(k) clearances |
| Oct 15, 2003 | DEROYAL POLY-REINFORCED SURGICAL GOWNS (STERILE, NON-STERILE)K031408 · FYA | 510(k) clearances |
| Aug 11, 2003 | DEROYAL SURGICAL DRAPES BACKTABLE COVERK030908 · KKX | 510(k) clearances |
| Jun 13, 2002 | DEROYAL SURGICAL, UMBILICUPK020753 · KSR | 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
