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 DMG America and its 1 subsidiaries with 29 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 2018: Ecosite Bulk Fill.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, DMG America and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 31, 2018 | Ecosite Bulk FillK171772 · EBF | 510(k) clearances |
| Sep 30, 2016 | TempoCem ClearK160443 · EMA | 510(k) clearances |
| Feb 25, 2014 | RETRACTION PASTEK130580 · MVL | 510(k) clearances |
| Jul 11, 2013 | ETCH GELK131248 · KLE | 510(k) clearances |
| Jun 10, 2011 | TEMPOCEMK110759 · EMB | 510(k) clearances |
| Nov 17, 2010 | SA FLOWABLE ADHESIVEK102603 · EBF | 510(k) clearances |
| Sep 28, 2010 | LUXATEMP ULTRA /STARK101710 · EBG | 510(k) clearances |
| Mar 26, 2010 | INFILTRATION KITK100062 · EBC | 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
