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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
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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
557812771

Catalogue (1719)

Page 3 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System ASFR4010
FDA UDI
Class IIActive
Chaorum Implant System ASFR4514S
FDA UDI
Class IIActive
Chaorum Implant System MSDH60357
FDA UDI
Class IIActive
Chaorum Implant System MSBA3515M
FDA UDI
Class IIActive
Chaorum Implant System CSAA35153M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45454
FDA UDI
Class IIActive
UD Implant System SDTH6354
FDA UDI
Class IIActive
Chaorum Implant System ATFS3614
FDA UDI
Class IIActive
Chaorum Implant System MSDH35104M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55154
FDA UDI
Class IIActive
UD Implant System MSTA4010MN
FDA UDI
Class IIActive
Chaorum Implant System ASFW6014
FDA UDI
Class IIActive
Chaorum Implant System ASFS3612
FDA UDI
Class IIActive
Chaorum Implant System MSDN65154
FDA UDI
Class IIActive
Chaorum Implant System CSAA55155N
FDA UDI
Class IIActive
Chaorum Implant System STA5525N
FDA UDI
Class IIActive
Chaorum Implant System MSDH50357
FDA UDI
Class IIActive
Chaorum Implant System MSCA4025M
FDA UDI
Class IIActive
Chaorum Implant System MSDH55357
FDA UDI
Class IIActive
Chaorum Implant System MSMA5025N
FDA UDI
Class IIActive
Chaorum Implant System MSMA4530N
FDA UDI
Class IIActive
UD Implant System UAAN45251
FDA UDI
Class IIActive
Chaorum Implant System CSAA50251N
FDA UDI
Class IIActive
Chaorum Implant System MSF3008M
FDA UDI
Class IIActive
Chaorum Implant System MSDH45105
FDA UDI
Class IIActive
Chaorum Implant System ASFW6012S
FDA UDI
Class IIActive
Chaorum Implant System SFBS3612M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65557
FDA UDI
Class IIActive
Chaorum Implant System MSDN45454M
FDA UDI
Class IIActive
UD Implant System SDTH4257M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40154MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA60154
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45157M
FDA UDI
Class IIActive
Chaorum Implant System MSMA5510N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45171MN
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55557
FDA UDI
Class IIActive
Chaorum Implant System MSDN45454
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65257
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40354M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65254
FDA UDI
Class IIActive
UD Implant System SDTN610
FDA UDI
Class IIActive
UD Implant System UAAH55254
FDA UDI
Class IIActive
UD Implant System SDTN445
FDA UDI
Class IIActive
Chaorum Implant System CSAA45173M
FDA UDI
Class IIActive
Chaorum Implant System PSFS3515M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50554
FDA UDI
Class IIActive
UD Implant System SCTT510
FDA UDI
Class IIActive
Chaorum Implant System MSDH65454
FDA UDI
Class IIActive
Chaorum Implant System MSMA5010H
FDA UDI
Class IIActive
Chaorum Implant System CSAA50171
FDA UDI
Class IIActive

Related Companies

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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