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 14, 2026, FDA's public records list Pioneering Technologies, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Sep 22, 1992: ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF.
| Sep 22, 1992 | ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIFK922025 · DSY | 510(k) clearances |
| Feb 14, 1992 | PTI ANNULOPLASTY RING(STERILE)K905175 · KRH | 510(k) clearances |
| Dec 31, 1991 | PTI INTRA-ART (TM) PICK-UP WICKSK905068 · EFQ | 510(k) clearances |
| May 6, 1991 | PTI STERNAL CLOSURE WIRE SUTUREK910067 · GAQ | 510(k) clearances |
| Mar 18, 1991 | PTI ANASTOMARK FLEXIBLE CORONARY BYPASS GRAFTK905067 · DSY | 510(k) clearances |
| Jul 3, 1990 | MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARYK901815 · DRE | 510(k) clearances |
| Jul 3, 1990 | PTI ANASTOMARK(TM) CORONARY BYPASS GRAFT MARKERSK901682 · DSY | 510(k) clearances |
| Jun 20, 1990 | PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBEK901531 · DNP | 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
