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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 19 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System ATFW5014
FDA UDI
Class IIActive
Chaorum Implant System ATFR4010S
FDA UDI
Class IIActive
Chaorum Implant System MSMA4510H
FDA UDI
Class IIActive
Chaorum Implant System MSAA60152
FDA UDI
Class IIActive
Chaorum Implant System PSFW6010S
FDA UDI
Class IIActive
Chaorum Implant System MSCAS6025
FDA UDI
Class IIActive
Chaorum Implant System MSDN60357
FDA UDI
Class IIActive
Chaorum Implant System CSAA45153MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN65455
FDA UDI
Class IIActive
Chaorum Implant System STA3535MH
FDA UDI
Class IIActive
Chaorum Implant System MSAA55251N
FDA UDI
Class IIActive
UD Implant System SDTH545
FDA UDI
Class IIActive
UD Implant System UDS6010M
FDA UDI
Class IIActive
UD Implant System SCTT415M
FDA UDI
Class IIActive
Chaorum Implant System MSDH45554
FDA UDI
Class IIActive
Chaorum Implant System MSBA3550M
FDA UDI
Class IIActive
Chaorum Implant System ATFW5012
FDA UDI
Class IIActive
Chaorum Implant System ATFS3612MS
FDA UDI
Class IIActive
Chaorum Implant System SFBR4508
FDA UDI
Class IIActive
Chaorum Implant System STA4515MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA40255M
FDA UDI
Class IIActive
Chaorum Implant System MSAA35151M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40251MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA50254
FDA UDI
Class IIActive
Chaorum Implant System MSDN45457M
FDA UDI
Class IIActive
Chaorum Implant System CSAA55152
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45357M
FDA UDI
Class IIActive
Chaorum Implant System MSMA4015N
FDA UDI
Class IIActive
Chaorum Implant System BAH00
FDA UDI
Class IIActive
Chaorum Implant System MSAA45173MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA40154M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45171M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45155N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS3545M
FDA UDI
Class IIActive
Chaorum Implant System MDH4035M
FDA UDI
Class IIActive
UD Implant System SDTH455
FDA UDI
Class IIActive
Chaorum Implant System CSAA40175MN
FDA UDI
Class IIActive
UD Implant System SDTN40357M
FDA UDI
Class IIActive
Chaorum Implant System STA5050N
FDA UDI
Class IIActive
Chaorum Implant System MSBA4045
FDA UDI
Class IIActive
Chaorum Implant System CSAA60252N
FDA UDI
Class IIActive
UD Implant System UAAN45153
FDA UDI
Class IIActive
Chaorum Implant System ASFS3614M
FDA UDI
Class IIActive
Chaorum Implant System MSAA55154
FDA UDI
Class IIActive
UD Implant System SDTH00
FDA UDI
Class IIActive
UD Implant System SBA3545
FDA UDI
Class IIActive
UD Implant System UDS4010M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45253N
FDA UDI
Class IIActive
Chaorum Implant System STA4555MN
FDA UDI
Class IIActive
Chaorum Implant System MPUN
FDA UDI
Class IActive

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