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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 9 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System STA4520H
FDA UDI
Class IIActive
Chaorum Implant System MSMA3525MH
FDA UDI
Class IIActive
Chaorum Implant System STA3550MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH35354M
FDA UDI
Class IIActive
UD Implant System SDTN40557M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40171MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA50252N
FDA UDI
Class IIActive
UD Implant System SDTH5157
FDA UDI
Class IIActive
Chaorum Implant System MSAA40252MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN45157
FDA UDI
Class IIActive
Chaorum Implant System MSDH40455M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45154M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50155
FDA UDI
Class IIActive
UD Implant System SDTH4557
FDA UDI
Class IIActive
UD Implant System UDH6545
FDA UDI
Class IIActive
Chaorum Implant System ASFS3612M
FDA UDI
Class IIActive
Chaorum Implant System MDH5010
FDA UDI
Class IIActive
Chaorum Implant System ASFS3016MS
FDA UDI
Class IIActive
Chaorum Implant System MSAA40155M
FDA UDI
Class IIActive
Chaorum Implant System STA3515MH
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60157
FDA UDI
Class IIActive
UD Implant System SDTN4055M
FDA UDI
Class IIActive
Chaorum Implant System STA4520MN
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50104
FDA UDI
Class IIActive
Chaorum Implant System MSDH40457M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40171M
FDA UDI
Class IIActive
UD Implant System MSCSM127
FDA UDI
Class IIActive
UD Implant System SDTN6457
FDA UDI
Class IIActive
UD Implant System UDH4035
FDA UDI
Class IIActive
Chaorum Implant System SCSRW
FDA UDI
Class IIActive
Chaorum Implant System CSAA50173N
FDA UDI
Class IIActive
Chaorum Implant System STA3525MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA55174
FDA UDI
Class IIActive
Chaorum Implant System ATFR4510
FDA UDI
Class IIActive
Chaorum Implant System CSAA45154MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA45175M
FDA UDI
Class IIActive
Chaorum Implant System MSAA60153
FDA UDI
Class IIActive
Chaorum Implant System MSDH65104
FDA UDI
Class IIActive
Chaorum Implant System MSDN40454M
FDA UDI
Class IIActive
UD Implant System UDH4025M
FDA UDI
Class IIActive
Chaorum Implant System MSBA4040M
FDA UDI
Class IIActive
Chaorum Implant System STA3540MH
FDA UDI
Class IIActive
Chaorum Implant System MSBA4015
FDA UDI
Class IIActive
Chaorum Implant System PSFR4008
FDA UDI
Class IIActive
Chaorum Implant System MSDN45154
FDA UDI
Class IIActive
Chaorum Implant System STA4025MN
FDA UDI
Class IIActive
Chaorum Implant System MDH6000
FDA UDI
Class IIActive
Chaorum Implant System ASFS3610S
FDA UDI
Class IIActive
Chaorum Implant System CSAA55173
FDA UDI
Class IIActive
Chaorum Implant System MSDH50454
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