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Sign in to claim this brandDM CEOSA
Spain·ES-MF-000000579
Last updated September 18, 2026
What DM CEOSA makes
The company manufactures orthodontic appliances, including soldered bracket systems (e.g., Roth, Rickettts, and Cervera designs) for dental arches, lingual hooks and retainers, and specialized tubing for bonding and soldering. Their portfolio also includes soldering plates, double-conversion molar tubes, and a C-Modeler class II+ device for dental modeling. These products are primarily used in fixed orthodontic treatments and dental laboratory procedures.
The devices fall under EU Medical Device Regulation classifications of Class I and Class IIa, with all products listed in the EUDAMED database. The manufacturer is based in Spain and adheres to EU regulatory requirements for medical devices in dentistry.
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 DM CEOSA manufacture?
DM CEOSA specializes in orthodontic appliances, including soldered bracket systems like Roth, Ricketts, and Cervera designs for dental arches. Their portfolio also covers lingual hooks, retainers, specialized tubing for bonding and soldering, and tools like the C-Modeler class II+ device for dental modeling. These products are primarily used in fixed orthodontic treatments and dental laboratory procedures.
Where is DM CEOSA based?
DM CEOSA is based in Spain, where it operates under EU regulatory requirements for medical devices. This location ensures compliance with the European Union’s standards for orthodontic and dental laboratory products.
Which regulatory registries list DM CEOSA’s devices?
All of DM CEOSA’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This listing confirms their availability under EU regulatory oversight, though individual device compliance depends on their classification and conformity assessment.
How are DM CEOSA’s devices classified under EU regulations?
DM CEOSA’s devices fall under Class I and Class IIa classifications under the EU Medical Device Regulation. Class I includes lower-risk items like soldering plates and brackets, while Class IIa covers slightly higher-risk products like the C-Modeler class II+ device, which requires additional conformity assessment steps to ensure safety and performance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Spain
- Address
- 18-20, Aeronautica , Alcorcon, Spain
- Website
- dmceosa.com
This website did not respond when we last checked — the domain may no longer be active. Last checked 2026-09-18.
- —
- —
- [email protected]
- Phone
- +34 916441276
- PRRC Contact
- Ana Maria Perez Perez
- EUDAMED SRN
- ES-MF-000000579
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (1103)
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