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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
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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 2 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System CSAA60175
FDA UDI
Class IIActive
Chaorum Implant System STA3555MN
FDA UDI
Class IIActive
Chaorum Implant System ASFS3008MS
FDA UDI
Class IIActive
Chaorum Implant System MDH5000
FDA UDI
Class IIActive
Chaorum Implant System MSDH65557
FDA UDI
Class IIActive
Chaorum Implant System MSBA3535M
FDA UDI
Class IIActive
Chaorum Implant System ASFW5014S
FDA UDI
Class IIActive
Chaorum Implant System PSFR4510
FDA UDI
Class IIActive
Chaorum Implant System MSDH65554
FDA UDI
Class IIActive
UD Implant System UDH6535
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60457
FDA UDI
Class IIActive
Chaorum Implant System MSCAS35554M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45354
FDA UDI
Class IIActive
Chaorum Implant System CSAA60153N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65157
FDA UDI
Class IIActive
UD Implant System SDTN410
FDA UDI
Class IIActive
UD Implant System SCTT4045M
FDA UDI
Class IIActive
Chaorum Implant System MSAA50153N
FDA UDI
Class IIActive
UD Implant System UAAN45252
FDA UDI
Class IIActive
Chaorum Implant System STA3530MH
FDA UDI
Class IIActive
Chaorum Implant System ATFS3614MS
FDA UDI
Class IIActive
Chaorum Implant System STA3555MH
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45157
FDA UDI
Class IIActive
Chaorum Implant System SFBS3608M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60555
FDA UDI
Class IIActive
Chaorum Implant System MSMA6525H
FDA UDI
Class IIActive
UD Implant System SDTH445
FDA UDI
Class IIActive
Chaorum Implant System CSAA40155M
FDA UDI
Class IIActive
Chaorum Implant System MSF4008
FDA UDI
Class IIActive
Chaorum Implant System MSAA55251
FDA UDI
Class IIActive
UD Implant System UDH4500M
FDA UDI
Class IIActive
Chaorum Implant System MSMA4525MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA55153
FDA UDI
Class IIActive
Chaorum Implant System MSMA4055MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA50174N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45255MN
FDA UDI
Class IIActive
UD Implant System UAAH55152
FDA UDI
Class IIActive
Chaorum Implant System MSDH45104M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45254MN
FDA UDI
Class IIActive
UD Implant System SMA4015H
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45554
FDA UDI
Class IIActive
Chaorum Implant System MSDH40255M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50457
FDA UDI
Class IIActive
UD Implant System UDH4555
FDA UDI
Class IIActive
Chaorum Implant System MSF3510M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45105M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40151M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45104M
FDA UDI
Class IIActive
Chaorum Implant System MSDH55354
FDA UDI
Class IIActive
Chaorum Implant System MSDH60107
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