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Sign in to claim this brandBonesupport AB
US
Last updated May 23, 2026
What Bonesupport AB makes
The company produces synthetic bone matrix implants, including antimicrobial and non-antimicrobial variants, as well as moulds for creating synthetic bone graft beads. These products are designed for bone void filling and grafting applications, such as reconstructive and trauma surgery.
The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with submissions documented via FDA 510(k) and FDA UDI registries. The company 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 types of medical devices does Bonesupport AB manufacture?
Bonesupport AB specializes in synthetic bone matrix implants, including both antimicrobial and non-antimicrobial versions. Their portfolio also includes moulds for creating synthetic bone graft beads. These devices are primarily used in procedures like reconstructive and trauma surgery to fill bone voids or support grafting.
Where is Bonesupport AB based?
Bonesupport AB is headquartered in the United States. The company’s location is relevant for understanding its regulatory submissions and compliance with U.S. medical device regulations.
Which regulatory registries list Bonesupport AB’s devices?
Bonesupport AB’s devices are documented in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries track submissions and compliance for Class I and Class II devices, ensuring traceability and regulatory oversight.
How are Bonesupport AB’s devices classified under medical device regulations?
Bonesupport AB’s devices fall into two regulatory classes: Class I (generally lower-risk products) and Class II (moderate-risk devices requiring special controls). Classification determines the level of scrutiny and regulatory pathways, such as 510(k) submissions, required for market authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cerament™|bead Tray | A0513 | FDA UDI | Class I | Active |
| Cerament® G | A0535-06 | FDA UDI | Class II | Active |
| Cerament™bone Void Filler | A0210-08 | FDA UDI | Class II | Active |
| Cerament™bone Void Filler | A0210-09 | FDA UDI | Class II | Active |
| Cerament® G | A0450-11 | FDA UDI | Class II | Active |
| Cerament® G | A0535-05 | FDA UDI | Class II | Active |
| Cerament™bone Void Filler | A0210-11 | FDA UDI | Class II | Active |
| Cerament G | DEN210044 | FDA 510(k)FDA UDI | Class II | Active |
| Cerament Bone Void Filler | K201535 | FDA 510(k) | Class II | Active |
| Cerament Bone Void Filler | K240459 | FDA 510(k) | Class II | Active |
| Cerament Bone Void Filler, Model A0210 | K073316 | FDA 510(k) | Class II | Active |
| Cerament G | K234008 | FDA 510(k) | Class II | Active |
| Cerament Bone Void Filler | K051951 | FDA 510(k) | Class II | Active |
| Cerament Ibone Void Filler High Contrast, Model A 0210-12 | K090871 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Bone Support Ab LUND Skane · SE FEI 3005304945