Curasan AG
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181721 | Ceracell Ortho Foam | MQV | 2018-09-17 | View |
| 510(k) | K160566 | Cerasorb Ortho Foam | MQV | 2016-12-02 | View |
| 510(k) | K111105 | CURASAN OSSEOLIVE DENTAL | LYC | 2012-12-20 | View |
| 510(k) | K103709 | CERACELL DENTAL | LYC | 2011-03-10 | View |
| 510(k) | K102872 | OSBONE DENTAL | LYC | 2011-01-12 | View |
| 510(k) | K100841 | BONEOPTIMIZER | MQV | 2010-08-19 | View |
| 510(k) | K063106 | REVOIS IMPLANT SYSTEM | NHA | 2007-06-11 | View |
| 510(k) | K040216 | CERASORB M ORTHO | MQV | 2004-03-26 | View |
| 510(k) | K031651 | MODIFICATION TO CERASORB ORTHO | MQV | 2003-08-13 | View |
| 510(k) | K014156 | CERASORB ORTHO | MQV | 2002-03-18 | View |
No matching devices.
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