Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in LiechtensteinLabelled 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 Ivoclar and its 3 subsidiaries with 193 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Dec 16, 2015: Zenostar MT, Zenostar Color Liquids.
| Dec 16, 2015 | Zenostar MT, Zenostar Color LiquidsK152118 · EIH | 510(k) clearances |
| Oct 7, 2015 | Helioseal F Sealant Refill 1 x 1.25 g, REF 558519AN, and Helioseal F Assortment (kit) 5 x 1.25 g, REF 558518AN. Dental sealant. -- ivoclarClass II · A defect occurred in the production process of Helioseal F Sealant; the particles in the faulty component seem to be lar | Device recalls |
| Aug 13, 2015 | IVOBASE CAD FOR ZENOTEC, IVOBASE CAD BOND, IVOBASE CAD MODELLING LIQUIDK151142 · EBI | 510(k) clearances |
| Jan 5, 2015 | zenostar MO, Zenostar T, Zenostar VisualiZrK142233 · EIH | 510(k) clearances |
| May 24, 2013 | ZENOLUXK130184 · EIH | 510(k) clearances |
| Oct 17, 2011 | ZENOTEC ZR BRIDGE, ZENOSTAR ZR TRANSLUCENT, ZENOTEC COLOR ZR, ZENOSTAR COLOR ZRK112710 · EIH | 510(k) clearances |
| Mar 16, 2011 | ZENOFLEX DIMENSIONK103773 · EIH | 510(k) clearances |
| Feb 16, 2011 | ZENOSTAR MAGIC GLAZEK103494 · EIH | 510(k) clearances |
| Sep 18, 2008 | ZENO AI ECO DISCK082257 · 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
