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 Jensen Industries with 17 510(k) clearances. The most recent is a 510(k) clearance dated Mar 20, 2019: Jensen Shade Effect Liquids.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 20, 2019 | Jensen Shade Effect LiquidsK183408 · EIH | 510(k) clearances |
| Dec 18, 2014 | INSYNC ZR HIGH TRANSLUCENCY ZIRCONIAK142043 · EIH | 510(k) clearances |
| Dec 1, 2011 | JENSEN ZIRCONIAK112806 · EIH | 510(k) clearances |
| Sep 14, 2011 | THE INSYNC CERAMIC SYSTEMK111743 · EIH | 510(k) clearances |
| Mar 1, 2007 | CREATION CP-ZI PORCELAINK070114 · EIH | 510(k) clearances |
| May 4, 2005 | THE LF-P CERAMIC SYSTEMK050838 · EIH | 510(k) clearances |
| Jan 11, 2005 | WILLI GELLER CREATION ZI PORCELAINK043201 · EIH | 510(k) clearances |
| Dec 20, 2004 | WILLI GELLER CREATION CP PORCELAINK043221 · EIH | 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
