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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 14 of 35
DeviceModel / ReferenceRegistriesClassStatus
UD Implant System SDTN435M
FDA UDI
Class IIActive
UD Implant System SDTH6454
FDA UDI
Class IIActive
Chaorum Implant System MDH4000
FDA UDI
Class IIActive
UD Implant System UAAN55253
FDA UDI
Class IIActive
Chaorum Implant System MSDN45104M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS5025
FDA UDI
Class IIActive
Chaorum Implant System CSAA60174N
FDA UDI
Class IIActive
Chaorum Implant System MSDN50104
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55157
FDA UDI
Class IIActive
UD Implant System SDTH00M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40173M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45557
FDA UDI
Class IIActive
Chaorum Implant System MSDH55104
FDA UDI
Class IIActive
UD Implant System SCTT425M
FDA UDI
Class IIActive
Chaorum Implant System MSDN65554
FDA UDI
Class IIActive
Chaorum Implant System MSCA6555
FDA UDI
Class IIActive
Chaorum Implant System MSF6007
FDA UDI
Class IIActive
Chaorum Implant System MSDH60354
FDA UDI
Class IIActive
Chaorum Implant System MDH6055
FDA UDI
Class IIActive
Chaorum Implant System ATFR4512S
FDA UDI
Class IIActive
Chaorum Implant System MSBA4030M
FDA UDI
Class IIActive
UD Implant System UDH5500
FDA UDI
Class IIActive
Chaorum Implant System MSDN55255
FDA UDI
Class IIActive
Chaorum Implant System MSCA4535
FDA UDI
Class IIActive
Chaorum Implant System MSAA60154N
FDA UDI
Class IIActive
Chaorum Implant System MDH5510
FDA UDI
Class IIActive
Chaorum Implant System MSMA5025H
FDA UDI
Class IIActive
Chaorum Implant System CSAA45251MN
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4512
FDA UDI
Class IIActive
Chaorum Implant System MDH3500M
FDA UDI
Class IIActive
UD Implant System SDTN545
FDA UDI
Class IIActive
UD Implant System SDTN415
FDA UDI
Class IIActive
UD Implant System SDTH4025M
FDA UDI
Class IIActive
UD Implant System UDH6555
FDA UDI
Class IIActive
Chaorum Implant System STA5520H
FDA UDI
Class IIActive
Chaorum Implant System STA4525H
FDA UDI
Class IIActive
Chaorum Implant System SCSS00
FDA UDI
Class IIActive
Chaorum Implant System MSAA50252
FDA UDI
Class IIActive
Chaorum Implant System MSDN45455M
FDA UDI
Class IIActive
Chaorum Implant System STA4545N
FDA UDI
Class IIActive
Chaorum Implant System CSAA45251M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60257
FDA UDI
Class IIActive
UD Implant System SDTH5554
FDA UDI
Class IIActive
Chaorum Implant System CSAA55153N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45253N
FDA UDI
Class IIActive
Chaorum Implant System MDH4025M
FDA UDI
Class IIActive
Chaorum Implant System MSAA60253
FDA UDI
Class IIActive
Chaorum Implant System STA5545N
FDA UDI
Class IIActive
Chaorum Implant System CSAA45254N
FDA UDI
Class IIActive
Chaorum Implant System STA4510H
FDA UDI
Class IIActive

Related Companies

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Authorities

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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