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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 18 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System PSFR4011S
FDA UDI
Class IIActive
Chaorum Implant System MSDH45357M
FDA UDI
Class IIActive
Chaorum Implant System MDH4525M
FDA UDI
Class IIActive
UD Implant System SMA4015MN
FDA UDI
Class IIActive
Chaorum Implant System MSF5013
FDA UDI
Class IIActive
Chaorum Implant System CSAA45174MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA45175
FDA UDI
Class IIActive
Chaorum Implant System MSAA45175MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA45253M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55254
FDA UDI
Class IIActive
Chaorum Implant System ASFS3612S
FDA UDI
Class IIActive
Chaorum Implant System STA4045MH
FDA UDI
Class IIActive
Chaorum Implant System CSAA45153M
FDA UDI
Class IIActive
Chaorum Implant System MSAA50255
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4010
FDA UDI
Class IIActive
Chaorum Implant System MDH6500
FDA UDI
Class IIActive
Chaorum Implant System CSAA35151M
FDA UDI
Class IIActive
UD Implant System SDTH645
FDA UDI
Class IIActive
Chaorum Implant System MSDH45457M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40251MN
FDA UDI
Class IIActive
UD Implant System SDTH4045M
FDA UDI
Class IIActive
Chaorum Implant System MDH8545
FDA UDI
Class IIActive
Chaorum Implant System PSFW6008S
FDA UDI
Class IIActive
Chaorum Implant System ATFS3610
FDA UDI
Class IIActive
Chaorum Implant System STA4030MH
FDA UDI
Class IIActive
UD Implant System SDTN4357
FDA UDI
Class IIActive
Chaorum Implant System MDH5555
FDA UDI
Class IIActive
Chaorum Implant System ASFR4508
FDA UDI
Class IIActive
Chaorum Implant System MSDN55154
FDA UDI
Class IIActive
Chaorum Implant System PSFS3010MS
FDA UDI
Class IIActive
Chaorum Implant System STA4540N
FDA UDI
Class IIActive
Chaorum Implant System PSFR4507
FDA UDI
Class IIActive
Chaorum Implant System MSDH35554M
FDA UDI
Class IIActive
Chaorum Implant System MSF5011
FDA UDI
Class IIActive
UD Implant System UAAH55253
FDA UDI
Class IIActive
Chaorum Implant System MSAA60252N
FDA UDI
Class IIActive
Chaorum Implant System MSDH45107M
FDA UDI
Class IIActive
UD Implant System SDTH5354
FDA UDI
Class IIActive
UD Implant System UAAH45151M
FDA UDI
Class IIActive
UD Implant System UDS4013M
FDA UDI
Class IIActive
Chaorum Implant System MSMA3510MN
FDA UDI
Class IIActive
Chaorum Implant System PSFS3515MS
FDA UDI
Class IIActive
Chaorum Implant System MSDH45255
FDA UDI
Class IIActive
UD Implant System SDTH40257M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40107M
FDA UDI
Class IIActive
UD Implant System SBA3535M
FDA UDI
Class IIActive
Chaorum Implant System CSAA35154M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45155
FDA UDI
Class IIActive
Chaorum Implant System MSDN45257M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50557
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