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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 16 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSAA55252
FDA UDI
Class IIActive
Chaorum Implant System MSBA4025
FDA UDI
Class IIActive
Chaorum Implant System MSMA6510H
FDA UDI
Class IIActive
Chaorum Implant System MSDH45155M
FDA UDI
Class IIActive
UD Implant System SDTN4454
FDA UDI
Class IIActive
UD Implant System SDTN4107
FDA UDI
Class IIActive
Chaorum Implant System CSAA50155N
FDA UDI
Class IIActive
Chaorum Implant System MDH4000M
FDA UDI
Class IIActive
Chaorum Implant System STA5515N
FDA UDI
Class IIActive
Chaorum Implant System ATFR4508S
FDA UDI
Class IIActive
Chaorum Implant System CSAA50172N
FDA UDI
Class IIActive
Chaorum Implant System STA4530H
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45457
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50357
FDA UDI
Class IIActive
Chaorum Implant System MSMA6540N
FDA UDI
Class IIActive
Chaorum Implant System MSDH45354M
FDA UDI
Class IIActive
Chaorum Implant System ASFW6008
FDA UDI
Class IIActive
Chaorum Implant System ASFBW5010
FDA UDI
Class IIActive
Chaorum Implant System MSF6013
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60454
FDA UDI
Class IIActive
Chaorum Implant System MSAA55153
FDA UDI
Class IIActive
UD Implant System SDTN5257
FDA UDI
Class IIActive
Chaorum Implant System STA5045H
FDA UDI
Class IIActive
Chaorum Implant System MSDN55457
FDA UDI
Class IIActive
Chaorum Implant System MSAA60252
FDA UDI
Class IIActive
Chaorum Implant System MSDN65257
FDA UDI
Class IIActive
Chaorum Implant System MDH6515
FDA UDI
Class IIActive
Chaorum Implant System CSAA50254
FDA UDI
Class IIActive
Chaorum Implant System PSFR4015
FDA UDI
Class IIActive
Chaorum Implant System MSBA4035
FDA UDI
Class IIActive
Chaorum Implant System MSMA4525MH
FDA UDI
Class IIActive
Chaorum Implant System CSAA45151
FDA UDI
Class IIActive
UD Implant System SDTH5104
FDA UDI
Class IIActive
Chaorum Implant System MSCAS35154M
FDA UDI
Class IIActive
Chaorum Implant System STA4550H
FDA UDI
Class IIActive
Chaorum Implant System MSAA45153MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA50153
FDA UDI
Class IIActive
Chaorum Implant System MSDN40257M
FDA UDI
Class IIActive
Chaorum Implant System MSDN55555
FDA UDI
Class IIActive
UD Implant System SBA3535
FDA UDI
Class IIActive
Chaorum Implant System MSDH45555
FDA UDI
Class IIActive
UD Implant System SDTN425M
FDA UDI
Class IIActive
UD Implant System SDTN5154
FDA UDI
Class IIActive
Chaorum Implant System CSAA40253M
FDA UDI
Class IIActive
Chaorum Implant System MSMA4515MH
FDA UDI
Class IIActive
Chaorum Implant System ATFW6010S
FDA UDI
Class IIActive
Chaorum Implant System MSDN55355
FDA UDI
Class IIActive
UD Implant System SDTN4015M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60172N
FDA UDI
Class IIActive
Chaorum Implant System STA5550N
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