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 Ethox Corp. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Mar 15, 2004: ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS.
| Mar 15, 2004 | ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFSK040286 · DXQ | 510(k) clearances |
| Oct 10, 2003 | CUF-COVER (TM)K031195 · DXQ | 510(k) clearances |
| Feb 21, 1997 | TUM-E-VACK962850 · KDH | 510(k) clearances |
| Sep 30, 1994 | NO-MESK935633 · KNT | 510(k) clearances |
| Dec 9, 1992 | TUM-E-VAC BITE BLOCKK921946 · JXL | 510(k) clearances |
| Sep 25, 1989 | PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK885220 · KNT | 510(k) clearances |
| Sep 11, 1989 | SURGI SQUEEZK894927 · KZD | 510(k) clearances |
| Feb 10, 1989 | SURGI-CUF STERILE/NON-STERILE DISPOSABLEK883977 · DXQ | 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
