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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 22 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSAA55155
FDA UDI
Class IIActive
Chaorum Implant System STA5540H
FDA UDI
Class IIActive
Chaorum Implant System CSAA50171N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45152MN
FDA UDI
Class IIActive
Chaorum Implant System SFBW6014
FDA UDI
Class IIActive
UD Implant System SDTN5254
FDA UDI
Class IIActive
Chaorum Implant System MSF3011M
FDA UDI
Class IIActive
Chaorum Implant System MSAA35151MN
FDA UDI
Class IIActive
Chaorum Implant System MDH5035
FDA UDI
Class IIActive
Chaorum Implant System ASFS3012M
FDA UDI
Class IIActive
Chaorum Implant System ATFW6010
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45457M
FDA UDI
Class IIActive
Chaorum Implant System MSMA6035N
FDA UDI
Class IIActive
Chaorum Implant System CSAA45251N
FDA UDI
Class IIActive
UD Implant System SDTH4157M
FDA UDI
Class IIActive
UD Implant System SDTH4154
FDA UDI
Class IIActive
Chaorum Implant System MSDN40105M
FDA UDI
Class IIActive
UD Implant System SDTH4107
FDA UDI
Class IIActive
UD Implant System UDS5008M
FDA UDI
Class IIActive
Chaorum Implant System ATFW5010S
FDA UDI
Class IIActive
Chaorum Implant System MSAA35154M
FDA UDI
Class IIActive
Chaorum Implant System MSDH55154
FDA UDI
Class IIActive
Chaorum Implant System STA5020N
FDA UDI
Class IIActive
Chaorum Implant System MDH4515M
FDA UDI
Class IIActive
Chaorum Implant System MSMA3525MN
FDA UDI
Class IIActive
Chaorum Implant System ATFS3610M
FDA UDI
Class IIActive
UD Implant System UAAH45254M
FDA UDI
Class IIActive
Chaorum Implant System MSF3508M
FDA UDI
Class IIActive
Chaorum Implant System MSCA6545
FDA UDI
Class IIActive
Chaorum Implant System STA3530MN
FDA UDI
Class IIActive
UD Implant System UDH4545
FDA UDI
Class IIActive
UD Implant System SBA3555
FDA UDI
Class IIActive
Chaorum Implant System MSDN65255
FDA UDI
Class IIActive
Chaorum Implant System MSDN40357M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60554
FDA UDI
Class IIActive
Chaorum Implant System MSBA4020M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45252MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA50254N
FDA UDI
Class IIActive
Chaorum Implant System MSMA3515MH
FDA UDI
Class IIActive
Chaorum Implant System ATFR4012S
FDA UDI
Class IIActive
Chaorum Implant System MSMA4045MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH55255
FDA UDI
Class IIActive
UD Implant System UDH5525
FDA UDI
Class IIActive
Chaorum Implant System MSAA60151
FDA UDI
Class IIActive
UD Implant System SCTT610
FDA UDI
Class IIActive
UD Implant System SDTH555
FDA UDI
Class IIActive
Chaorum Implant System MSDH50554
FDA UDI
Class IIActive
Chaorum Implant System MPUH
FDA UDI
Class IActive
Chaorum Implant System MSCAS45557
FDA UDI
Class IIActive
UD Implant System UDH4045M
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