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Sign in to claim this brandDoxa Dental AB
US
Last updated May 29, 2026
What Doxa Dental AB makes
Doxa Dental AB manufactures dental materials and related tools, including glass ionomer cement and composite resin products such as the Ceramir Bioceramic Implant Cement QuikCap and Ceramir® Restore QuikCap. The company also supplies single‑use application instruments like the Ceramir® Protect LC Syringe and various Ceramir Crown & Bridge QuikCap and QuikMix kits for restorative procedures.
These products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) database and the FDA UDI system. Doxa Dental AB is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Doxa Dental AB make?
Doxa Dental AB manufactures dental materials and related tools, including glass ionomer dental cement, dental composite resin, and single-use dental material application tools. Examples include Ceramir Bioceramic Implant Cement QuikCap, Ceramir® Restore QuikCap, Ceramir® Protect LC Syringe, and various Ceramir Crown & Bridge QuikCap and QuikMix kits used in restorative dental procedures.
Where is Doxa Dental AB based?
Doxa Dental AB is based in the United States, as stated in the company summary which confirms its location within the US.
Which regulatory registries list Doxa Dental AB's devices?
Doxa Dental AB's devices are listed in the FDA 510(k) database and the FDA UDI (Unique Device Identification) system, as indicated in the LISTED IN field of the device data.
How are Doxa Dental AB's devices classified?
Doxa Dental AB's devices are regulated as Class I and Class II medical devices, reflecting varying levels of risk and regulatory control, with Class II devices requiring special controls such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- ceramirus.com
- —
- —
- [email protected]
- Phone
- 1.855.369-2872
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 350486340
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ceramir Bioceramic Implant Cement QuikCap | 40037 | FDA UDI | Class II | Active |
| Ceramir® Restore QuikCap | 40039 | FDA UDI | Class II | Active |
| Ceramir® Protect LC Syringe | 40044 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikCap | 40028 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikCap | 40030 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikMix | 40034 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikCap | 40035 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikCap | 40031 | FDA UDI | Class II | Active |
| Ceramir Applicator 2 | 40027 | FDA UDI | Class I | Active |
| Ceramir Crown & Bridge QuikMix | 40032 | FDA UDI | Class II | Active |
| Ceramir® Protect LC Syringe | 40045 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikCap | 40029 | FDA UDI | Class II | Active |
| Ceramir® Restore QuikCap | 40038 | FDA UDI | Class II | Active |
| Ceramir Crown & Bridge QuikMix | 40033 | FDA UDI | Class II | Active |
| Xeracem | K081405 | FDA 510(k) | Class II | Active |
| Ceramir Restore QuikCap | K201937 | FDA 510(k) | Class II | Active |
| Ceramir Crown & Bridge | K113040 | FDA 510(k) | Class II | Active |
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