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US
Last updated May 23, 2026
What FOUNDATION FOR COMMUNITY BLOOD CENTER/COMMUNITY TISSUE SERVICES, THE makes
The company produces dental bone matrix implants derived from animal sources, designed to support bone regeneration in oral and maxillofacial procedures. These implants are intended for use in grafting applications where natural bone structure needs enhancement or restoration.
The portfolio consists of Class II devices, authorised under FDA regulations and listed in the FDA’s Unique Device Identifier (UDI) system. The manufacturer operates within the United States, adhering to applicable domestic regulatory requirements for medical devices.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Foundation for Community Blood Center/Community Tissue Services, The primarily manufacture?
The company specialises in dental bone matrix implants derived from animal sources. These implants are specifically designed to aid in bone regeneration during oral and maxillofacial procedures, such as grafting, where natural bone structure requires enhancement or restoration.
Where is Foundation for Community Blood Center/Community Tissue Services, The based, and does this affect the regulatory environment for their devices?
The company is based in the United States. Since their devices are authorised under FDA regulations, they must comply with domestic requirements for medical devices, including classification, listing, and UDI registration. The US regulatory framework governs their product development, manufacturing, and market introduction.
Which regulatory registries or databases list the devices manufactured by Foundation for Community Blood Center/Community Tissue Services, The?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) system. This database helps track and identify medical devices authorised for use in the US, ensuring transparency and traceability in the healthcare supply chain.
How are the devices produced by Foundation for Community Blood Center/Community Tissue Services, The classified under regulatory standards?
The company’s dental bone matrix implants fall under Class II device classification. This classification is determined by the FDA based on the level of risk associated with the device, requiring special controls in addition to general controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 071276372
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Maxxeus | XK010 | FDA UDI | Class II | Active |
| Maxxeus | XK020 | FDA UDI | Class II | Active |
| Maxxeus | XL020 | FDA UDI | Class II | Active |
| Maxxeus | XK005 | FDA UDI | Class II | Active |
| Maxxeus | XL040 | FDA UDI | Class II | Active |
| Maxxeus | OK025 | FDA UDI | Class II | Active |
| Maxxeus | OK005 | FDA UDI | Class II | Active |
| Maxxeus | OL005 | FDA UDI | Class II | Active |
| Maxxeus | XK040 | FDA UDI | Class II | Active |
| Maxxeus | XL080 | FDA UDI | Class II | Active |
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