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 Sulzer Intratherapeutics with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 13, 2002: MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY.
| Dec 13, 2002 | MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK023243 · FGE | 510(k) clearances |
| Jun 21, 2002 | MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK021729 · FGE | 510(k) clearances |
| May 31, 2002 | INTRACOIL SELF-EXPANDING PERIPHERAL STENTK021563 · JCT | 510(k) clearances |
| Apr 16, 2002 | INTRASTENT LD (LARGE DIAMETER) STENTK020528 · FGE | 510(k) clearances |
| Jan 17, 2002 | MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK014136 · FGE | 510(k) clearances |
| Sep 7, 2001 | PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK011806 · FGE | 510(k) clearances |
| Aug 23, 2001 | PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK012347 · FGE | 510(k) clearances |
| Aug 1, 2001 | PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYK012066 · FGE | 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
