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Sign in to claim this brandNobel Biocare AB
Sweden·SE-MF-000000009
Last updated September 17, 2026
What Nobel Biocare AB makes
Nobel Biocare AB manufactures single-use dental implant suprastructures, including temporary preformed components like screwdrivers, try-in screws, and replica implants for prosthetic fitting. Their portfolio also includes carbide dental burs designed for one-time use in dental procedures, as well as guided components such as base replicas, protection analogs, and guide pins for implant placement and verification.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb, with all relevant products registered in the EUDAMED database. Nobel Biocare AB is headquartered in Sweden.
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 Nobel Biocare AB primarily manufacture?
Nobel Biocare AB specializes in dental implant-related devices, focusing on single-use components. Their portfolio includes temporary preformed dental implant suprastructures like screwdrivers, try-in screws, and replica implants used for prosthetic fitting. Additionally, they produce carbide dental burs for one-time use in dental procedures, as well as guided components such as base replicas, protection analogs, and guide pins for implant placement and verification.
Where is Nobel Biocare AB based, and what does this mean for their regulatory compliance?
Nobel Biocare AB is headquartered in Sweden, which means their devices are subject to EU Medical Device Regulations (MDR). Since they manufacture products listed under Class I, Class IIa, and Class IIb, their devices must comply with these regulations and are registered in the EUDAMED database, the official EU registry for medical devices.
Which regulatory registries list Nobel Biocare AB’s devices, and why is this important?
Nobel Biocare AB’s devices are listed in the EUDAMED database, the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices under the EU Medical Device Regulations, allowing healthcare professionals, regulators, and patients to verify the legal status and classification of their products.
How are Nobel Biocare AB’s devices classified under EU regulations, and what does this classification indicate?
Nobel Biocare AB’s devices fall under Class I, Class IIa, and Class IIb classifications under the EU Medical Device Regulations. This classification determines the level of scrutiny and regulatory requirements for each product—Class I devices are generally low-risk, while Class IIa and IIb involve higher risks and require additional safety and performance evaluations before authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Sweden
- Address
- 1, Västra Hamngatan , Göteborg, Sweden
- Website
- nobelbiocare.com
- —
- —
- [email protected]
- Phone
- +1(800)322-5001
- PRRC Contact
- Stefan Trampler
- EUDAMED SRN
- SE-MF-000000009
- FDA FEI Number
- 3002807692
- DUNS Number
- 353939929
Catalogue (3532)
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Nobel Biocare AG US