Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Merz GroupLabelled 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 Merz Dental GmbH with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2017: PEEK Biosolution.
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.
| Dec 18, 2017 | PEEK BiosolutionK173124 · EBF | 510(k) clearances |
| Sep 15, 2014 | M-PM-DISC (PINK)K140758 · EBI | 510(k) clearances |
| Apr 11, 2014 | M-PM-DISCK134015 · MQC | 510(k) clearances |
| Aug 22, 2013 | PROMOLUX, PROMOLUX HI, WEROPRESS, PREMECO PCSK130076 · EBI | 510(k) clearances |
| May 21, 2012 | MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETHK120404 · ELM | 510(k) clearances |
| May 2, 2008 | ARTBLOC TEMP, DIMENSION: 15.5 X19.39 MM V-CLASSIC SHADES AND BLEACH SHADESK080556 · EBG | 510(k) clearances |
| Aug 21, 2007 | WIELAND ZENO CAO TEMPORARY PMMA DISC, TOOTH-COLOREDK071548 · EBG | 510(k) clearances |
| Sep 13, 2006 | ARTEGRAL IMCROWNK061809 · EBG | 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