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MICERIUM SPA

US

Last updated May 23, 2026

What MICERIUM SPA makes

Micerium SpA manufactures dental materials and tools for restorative and orthodontic procedures, including temporary orthodontic retainers, dental composite resins, and bonding agents for dentine. Their portfolio also includes professional abrasive materials for tooth preparation, reusable application tools, and single-use cannulas for material injection. Additional offerings comprise dental acrylic resins and abrasive disks designed for precision dental treatments.

The company’s devices are regulated under FDA’s UDI system, with classifications spanning Class I and Class II. Products are listed in the FDA’s Unique Device Identifier database, ensuring compliance with U.S. medical device regulations. The manufacturer 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 Micerium SpA primarily manufacture?

Micerium SpA specializes in dental materials and tools used in restorative and orthodontic treatments. Their portfolio includes temporary orthodontic retainers, dental composite resins, bonding agents for dentine, professional abrasive materials for tooth preparation, reusable application tools, single-use injection cannulas, dental acrylic resins, and abrasive disks. These products are designed to support precision dental procedures.

Where is Micerium SpA based, and how does this affect their regulatory compliance?

Micerium SpA is based in the United States, which means their devices must comply with U.S. medical device regulations. Their products are listed in the FDA’s Unique Device Identifier (UDI) system, ensuring traceability and regulatory transparency. This system helps track devices throughout their lifecycle, including manufacturing, distribution, and use.

Which regulatory registries or databases list Micerium SpA’s devices?

Micerium SpA’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry is part of the U.S. regulatory framework for medical devices, ensuring that each product has a unique identifier for tracking compliance, recalls, and post-market surveillance. Listing in this database is required for devices marketed in the U.S.

How are Micerium SpA’s devices classified under U.S. regulations?

Micerium SpA’s devices fall under FDA classifications of Class I and Class II. Class I devices generally pose minimal risk and may require general controls for regulation, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and oversight required for each product.

Why are some of Micerium SpA’s devices listed as single-use while others are reusable?

The distinction between single-use and reusable devices depends on their intended use, risk level, and sterilization feasibility. Single-use items like abrasive disks or injection cannulas are designed for one-time use to minimize infection risks and ensure sterility. Reusable tools, such as application instruments, are engineered to withstand sterilization processes, reducing waste and cost while maintaining safety standards for repeated use in clinical settings.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
—
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
436661136

Catalogue (679)

Page 3 of 14
DeviceModel / ReferenceRegistriesClassStatus
Ena Bond ® COSM300K
EUDAMEDFDA UDI
Class IIActive
Amcop Bioactivator BC3-DCM
FDA UDI
Class IActive
Amcop Bioactivator BSC3-DTM
FDA UDI
Class IActive
Ena Post CP1007
EUDAMEDFDA UDI
Class IActive
Amcop Bioactivator BF3-DEEPH
FDA UDI
Class IActive
Ena Shiny ESG10
FDA UDI
Class IActive
Ena HRI ® EHRBD3,5
EUDAMEDFDA UDI
Class IIActive
Ena HRI Flow EHR1F
FDA UDI
Class IIActive
Amcop Bioactivator BSC5-DTMH
FDA UDI
Class IActive
Ena HRI ® ERBF1
EUDAMEDFDA UDI
Class IIActive
Ena Bond ® COSM300A
FDA UDI
Class IIActive
Ena Cem Hf CPCZ
EUDAMEDFDA UDI
Class IIActive
Ena HRI ® EHRUE1
FDA UDI
Class IIActive
Ena HRI ® ETST
FDA UDI
Class IIActive
Universal 1 CU1UN
FDA UDI
Class IIActive
Universal 1 CU1OP
FDA UDI
Class IIActive
Enamel Plus Temp ® TEMPUD3
EUDAMEDFDA UDI
Class IIActive
Amcop Bioactivator BF4-DTM
FDA UDI
Class IActive
Amcop Bioactivator BIO-DCR1M
FDA UDI
Class IActive
Ena Etch ® COS101
FDA UDI
Class IIActive
Ena HRI ® EHRUD1
FDA UDI
Class IIActive
Amcop Bioactivator BF5-DCMH
FDA UDI
Class IActive
Ena HRI ® EHR3FC
EUDAMEDFDA UDI
Class IIActive
Temp Silicon Brush SS3
FDA UDI
Class IActive
Ena HRI ® EHRBD6
FDA UDI
Class IIActive
Amcop Bioactivator BF4-DCMH
FDA UDI
Class IActive
Ena HRI ® EHRBD4
EUDAMEDFDA UDI
Class IIActive
Ena HRI ® ERBD1
FDA UDI
Class IIActive
Ena HRI ® EHRTBD1
EUDAMEDFDA UDI
Class IIActive
Temp Silicon Brush SS5
FDA UDI
Class IActive
Ena HRI ® EHRUE1
EUDAMEDFDA UDI
Class IIActive
Amcop Bioactivator BF3-DEEP
FDA UDI
Class IActive
Amcop Bioactivator BIO-S4HM
FDA UDI
Class IActive
Amcop Bioactivator BIO-F5HM
FDA UDI
Class IActive
Amcop Bioactivator BSC5-DCM
FDA UDI
Class IActive
Amcop Bioactivator B0S1-DEEPH
FDA UDI
Class IActive
Ena HRI ® EHF6N
FDA UDI
Class IIActive
Ena HRI ® ERBF3
FDA UDI
Class IIActive
Amcop Bioactivator BIO-DCA1M
FDA UDI
Class IActive
Ena Shiny ESA
EUDAMEDFDA UDI
Class IActive
Amcop Bioactivator BIO-TC2HM
FDA UDI
Class IActive
Amcop Bioactivator BS3DTMH
FDA UDI
Class IActive
Ena HRI ® EHRUD6
EUDAMEDFDA UDI
Class IIActive
Ena Shiny ESFM
FDA UDI
Class IActive
Ena HRI ® EFFUD2
FDA UDI
Class IIActive
Ena Post CS050-2R
EUDAMEDFDA UDI
Class IActive
Amcop Bioactivator BIO-C5HM
FDA UDI
Class IActive
Enamel Plus Temp ® TEMP1N
FDA UDI
Class IIActive
Amcop Bioactivator BC3-DTM
FDA UDI
Class IActive
Ena Matrix ENAM
FDA UDI
Class IActive

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