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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 27 of 35
DeviceModel / ReferenceRegistriesClassStatus
UD Implant System SDTH615
FDA UDI
Class IIActive
Chaorum Implant System MSMA4035MH
FDA UDI
Class IIActive
Chaorum Implant System MSMA6540H
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50254
FDA UDI
Class IIActive
UD Implant System UAAN55254
FDA UDI
Class IIActive
Chaorum Implant System MSDN60255
FDA UDI
Class IIActive
Chaorum Implant System MSBA3540
FDA UDI
Class IIActive
Chaorum Implant System MSDH35454M
FDA UDI
Class IIActive
UD Implant System SDTN5554
FDA UDI
Class IIActive
Chaorum Implant System ASFW6008S
FDA UDI
Class IIActive
Chaorum Implant System ATFS3614S
FDA UDI
Class IIActive
Chaorum Implant System STA5040N
FDA UDI
Class IIActive
UD Implant System UDH5545
FDA UDI
Class IIActive
UD Implant System SDTN4157
FDA UDI
Class IIActive
UD Implant System UDH4525
FDA UDI
Class IIActive
Chaorum Implant System MSCA4525M
FDA UDI
Class IIActive
Chaorum Implant System MSDH40155M
FDA UDI
Class IIActive
UD Implant System SCTT535
FDA UDI
Class IIActive
UD Implant System SMA5530N
FDA UDI
Class IIActive
Chaorum Implant System MSDN50257
FDA UDI
Class IIActive
Chaorum Implant System STA4015MH
FDA UDI
Class IIActive
Chaorum Implant System MSBA4015M
FDA UDI
Class IIActive
Chaorum Implant System MSDN40154M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45151
FDA UDI
Class IIActive
Chaorum Implant System ASFW5008
FDA UDI
Class IIActive
Chaorum Implant System ASFR4014
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40257M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60175N
FDA UDI
Class IIActive
Chaorum Implant System ASFW6014S
FDA UDI
Class IIActive
Chaorum Implant System MSAA40153MN
FDA UDI
Class IIActive
Chaorum Implant System ASFR4012S
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55457
FDA UDI
Class IIActive
UD Implant System SMA4015N
FDA UDI
Class IIActive
Chaorum Implant System ASFS3016M
FDA UDI
Class IIActive
Chaorum Implant System MSDN60554
FDA UDI
Class IIActive
Chaorum Implant System MSAA40175MN
FDA UDI
Class IIActive
Chaorum Implant System ASFR4014S
FDA UDI
Class IIActive
Chaorum Implant System STA5515H
FDA UDI
Class IIActive
Chaorum Implant System CSAA40172MN
FDA UDI
Class IIActive
Chaorum Implant System PSFR4015S
FDA UDI
Class IIActive
Chaorum Implant System ASFBW6008
FDA UDI
Class IIActive
Chaorum Implant System MSMA5520H
FDA UDI
Class IIActive
UD Implant System SDTH435M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40457M
FDA UDI
Class IIActive
Chaorum Implant System MSDH65555
FDA UDI
Class IIActive
Chaorum Implant System MSAA45255
FDA UDI
Class IIActive
Chaorum Implant System PSFS3008M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45153
FDA UDI
Class IIActive
Chaorum Implant System MSAA45173M
FDA UDI
Class IIActive
UD Implant System SDTN415M
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