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 15, 2026, FDA's public records list Schneider International with 22 510(k) clearances. The most recent is a 510(k) clearance dated Jan 11, 1995: BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM.
| Jan 11, 1995 | BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEMK925406 · FGE | 510(k) clearances |
| Jun 23, 1993 | SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWIK931577 · DQX | 510(k) clearances |
| Jun 7, 1993 | SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIOK926271 · LIT | 510(k) clearances |
| Jun 7, 1993 | SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETERK926003 · DQO | 510(k) clearances |
| Feb 12, 1993 | SCHNEIDER HYDRO-SIL GUIDEWIREK925804 · DQX | 510(k) clearances |
| Dec 8, 1992 | SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETERK924591 · DQY | 510(k) clearances |
| Jul 21, 1992 | TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.K921856 · LIT | 510(k) clearances |
| Jun 17, 1992 | SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BALK921943 · LIT | 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
