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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Curasan and its 1 subsidiaries with 11 510(k) clearances and 2 warning letters. The most recent is a warning letter dated Jun 3, 2019: Warning letter: Medical Devices.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Curasan and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 3, 2019 | Warning letter: Medical DevicesCDRH | Warning letters |
| Sep 17, 2018 | Ceracell Ortho FoamK181721 · MQV | 510(k) clearances |
| Aug 23, 2017 | Warning letter: Complaint handling, MDR reporting, Design controlsCDRH | Warning letters |
| Dec 2, 2016 | Cerasorb Ortho FoamK160566 · MQV | 510(k) clearances |
| Dec 20, 2012 | CURASAN OSSEOLIVE DENTALK111105 · LYC | 510(k) clearances |
| Mar 10, 2011 | CERACELL DENTALK103709 · LYC | 510(k) clearances |
| Jan 12, 2011 | OSBONE DENTALK102872 · LYC | 510(k) clearances |
| Aug 19, 2010 | BONEOPTIMIZERK100841 · MQV | 510(k) clearances |
| Jun 11, 2007 | REVOIS IMPLANT SYSTEMK063106 · NHA | 510(k) clearances |
| Jul 22, 2005 | CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIOK051443 · LYC | 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
