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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
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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 20 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System ASFW6010S
FDA UDI
Class IIActive
Chaorum Implant System MSMA4045MN
FDA UDI
Class IIActive
UD Implant System SDTH6107
FDA UDI
Class IIActive
Chaorum Implant System CSAA50172
FDA UDI
Class IIActive
Chaorum Implant System MSDH65157
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60354
FDA UDI
Class IIActive
UD Implant System SDTH4254
FDA UDI
Class IIActive
Chaorum Implant System CSAA45151N
FDA UDI
Class IIActive
Chaorum Implant System ATFS3085MS
FDA UDI
Class IIActive
Chaorum Implant System SFBS3610M
FDA UDI
Class IIActive
Chaorum Implant System SFBS3612
FDA UDI
Class IIActive
UD Implant System UAAH55252
FDA UDI
Class IIActive
UD Implant System UDH4055
FDA UDI
Class IIActive
Chaorum Implant System MSDN65107
FDA UDI
Class IIActive
UD Implant System UDH4535M
FDA UDI
Class IIActive
Chaorum Implant System MSITH40ML
FDA UDI
Class IActive
Chaorum Implant System MSDN65157
FDA UDI
Class IIActive
Chaorum Implant System CSAA45174N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50107
FDA UDI
Class IIActive
UD Implant System UDH4535
FDA UDI
Class IIActive
Chaorum Implant System MSDH45254M
FDA UDI
Class IIActive
Chaorum Implant System ASFW5014
FDA UDI
Class IIActive
Chaorum Implant System CSAA45153N
FDA UDI
Class IIActive
Chaorum Implant System MSDN65555
FDA UDI
Class IIActive
Chaorum Implant System MSF3513M
FDA UDI
Class IIActive
UD Implant System SDTH4454
FDA UDI
Class IIActive
Chaorum Implant System MSAA55255N
FDA UDI
Class IIActive
Chaorum Implant System MSF6008
FDA UDI
Class IIActive
Chaorum Implant System MSAA50154N
FDA UDI
Class IIActive
Chaorum Implant System MSF5015
FDA UDI
Class IIActive
Chaorum Implant System MSCA4035M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55357
FDA UDI
Class IIActive
Chaorum Implant System MSMA6025H
FDA UDI
Class IIActive
Chaorum Implant System MSAA40151MN
FDA UDI
Class IIActive
Chaorum Implant System MSMA4515N
FDA UDI
Class IIActive
Chaorum Implant System PSFW6007
FDA UDI
Class IIActive
Chaorum Implant System MSCA4555M
FDA UDI
Class IIActive
Chaorum Implant System MDH5025
FDA UDI
Class IIActive
Chaorum Implant System MSMA4535MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN45254
FDA UDI
Class IIActive
Chaorum Implant System CSAA55173N
FDA UDI
Class IIActive
Chaorum Implant System SFBR4010
FDA UDI
Class IIActive
Chaorum Implant System MSDN60107
FDA UDI
Class IIActive
Chaorum Implant System ASFW6012
FDA UDI
Class IIActive
Chaorum Implant System MSDN40104M
FDA UDI
Class IIActive
UD Implant System SDTN4357M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45152
FDA UDI
Class IIActive
Chaorum Implant System MSDH65257
FDA UDI
Class IIActive
Chaorum Implant System MDH6015
FDA UDI
Class IIActive
UD Implant System SDTH40357M
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