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Medimecca Co., Ltd.

US

Last updated May 23, 2026

What Medimecca Co., Ltd. makes

Medimecca Co., Ltd. manufactures dental implant systems, including both the implant fixtures and temporary preformed suprastructures designed for single-use applications. Their portfolio includes the UD Implant System and multiple variants of the Chaorum Implant System, which are intended for dental restoration procedures.

The company’s devices are classified under FDA categories Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. Medimecca Co., Ltd. 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 Medimecca Co., Ltd. manufacture?

Medimecca Co., Ltd. specializes in dental implant solutions. Their portfolio includes dental implant systems, such as the UD Implant System, as well as temporary preformed suprastructures designed for single-use applications, like variants of the Chaorum Implant System. These devices are intended for dental restoration procedures, providing both the implant fixtures and temporary components to support healing and interim functionality.

Where is Medimecca Co., Ltd. based?

Medimecca Co., Ltd. is headquartered in the United States. The company’s location in the US aligns with its regulatory engagement, particularly in systems like the FDA’s UDI database, where its devices are listed for traceability and compliance.

Which regulatory registries list Medimecca Co., Ltd.’s devices?

Medimecca Co., Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track and identify medical devices throughout their lifecycle, ensuring transparency in regulatory oversight and market surveillance. Listing in this database is a key requirement for devices regulated by the FDA.

How are Medimecca Co., Ltd.’s devices classified under FDA regulations?

Medimecca Co., Ltd.’s devices fall into two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as dental implants.

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
—
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
557812771

Catalogue (1719)

Page 10 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System SFBS3012M
FDA UDI
Class IIActive
Chaorum Implant System ATFR4510S
FDA UDI
Class IIActive
Chaorum Implant System PSFW5013S
FDA UDI
Class IIActive
Chaorum Implant System STA4015MN
FDA UDI
Class IIActive
Chaorum Implant System PSFW6013
FDA UDI
Class IIActive
UD Implant System SDTN40157M
FDA UDI
Class IIActive
Chaorum Implant System STA4550N
FDA UDI
Class IIActive
Chaorum Implant System STA4510MN
FDA UDI
Class IIActive
Chaorum Implant System STA5010H
FDA UDI
Class IIActive
Chaorum Implant System MSMA5020H
FDA UDI
Class IIActive
Chaorum Implant System MSAA60153N
FDA UDI
Class IIActive
Chaorum Implant System MSDH65357
FDA UDI
Class IIActive
Chaorum Implant System CSAA40254M
FDA UDI
Class IIActive
Chaorum Implant System SFBS3614
FDA UDI
Class IIActive
Chaorum Implant System STA5050H
FDA UDI
Class IIActive
Chaorum Implant System MSDN50355
FDA UDI
Class IIActive
UD Implant System SDTH410M
FDA UDI
Class IIActive
UD Implant System SDTH4357M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3608S
FDA UDI
Class IIActive
Chaorum Implant System MSBA4010M
FDA UDI
Class IIActive
UD Implant System SDTH445M
FDA UDI
Class IIActive
UD Implant System UDS5013M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45152MN
FDA UDI
Class IIActive
Chaorum Implant System MSDH50355
FDA UDI
Class IIActive
Chaorum Implant System MSCAS5055
FDA UDI
Class IIActive
UD Implant System SDTN6357
FDA UDI
Class IIActive
Chaorum Implant System MDH4045
FDA UDI
Class IIActive
Chaorum Implant System MSAA50253
FDA UDI
Class IIActive
Chaorum Implant System PSFW5008S
FDA UDI
Class IIActive
Chaorum Implant System MSMA5530N
FDA UDI
Class IIActive
UD Implant System UAAN55153
FDA UDI
Class IIActive
Chaorum Implant System CSAA45254M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60152
FDA UDI
Class IIActive
Chaorum Implant System STA4540H
FDA UDI
Class IIActive
Chaorum Implant System MSAA45251N
FDA UDI
Class IIActive
Chaorum Implant System MSDN45557M
FDA UDI
Class IIActive
UD Implant System SDTH515
FDA UDI
Class IIActive
Chaorum Implant System PSFR4515
FDA UDI
Class IIActive
Chaorum Implant System MSDN45105
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50257
FDA UDI
Class IIActive
UD Implant System SDTH4010M
FDA UDI
Class IIActive
Chaorum Implant System MSAA55152
FDA UDI
Class IIActive
UD Implant System UDS4508M
FDA UDI
Class IIActive
UD Implant System SCTT455
FDA UDI
Class IIActive
UD Implant System SDTN5104
FDA UDI
Class IIActive
Chaorum Implant System MSAA45251
FDA UDI
Class IIActive
Chaorum Implant System MSDN60557
FDA UDI
Class IIActive
Chaorum Implant System MSDH45105M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3610MS
FDA UDI
Class IIActive
Chaorum Implant System STA3545MH
FDA UDI
Class IIActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Medimecca Co Ltd Seoul · KR FEI 3007649394