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 Dimensional Bioceramics, LLC with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 22, 2021: DB-EZ Bone Void Filler.
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.
| Sep 22, 2021 | DB-EZ Bone Void FillerK212353 · MQV | 510(k) clearances |
| Mar 15, 2021 | DB-CompositeK210193 · MQV | 510(k) clearances |
| Apr 22, 2020 | DB-OrthopedicsK200752 · MQV | 510(k) clearances |
| Jun 20, 2019 | DB-CMFK182742 · GXP | 510(k) clearances |
| Sep 25, 2017 | Dimensional Bioceramics Calcium Sulfate Device (DB-CSD)K171161 · MQV | 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