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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
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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 8 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSCAS45257M
FDA UDI
Class IIActive
Chaorum Implant System MDH6555
FDA UDI
Class IIActive
UD Implant System SMA5520N
FDA UDI
Class IIActive
Chaorum Implant System MSDN35555M
FDA UDI
Class IIActive
Chaorum Implant System MSDH45154M
FDA UDI
Class IIActive
Chaorum Implant System MSMA6040N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45153M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60255
FDA UDI
Class IIActive
Chaorum Implant System MSAA45171M
FDA UDI
Class IIActive
Chaorum Implant System STA4510N
FDA UDI
Class IIActive
UD Implant System UAAH45252
FDA UDI
Class IIActive
Chaorum Implant System PSFR4513S
FDA UDI
Class IIActive
Chaorum Implant System MSDH35154M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60357
FDA UDI
Class IIActive
Chaorum Implant System MSDH55155
FDA UDI
Class IIActive
Chaorum Implant System MSDH55554
FDA UDI
Class IIActive
UD Implant System SDTN635
FDA UDI
Class IIActive
Chaorum Implant System MDH4535
FDA UDI
Class IIActive
UD Implant System SBA3515M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55454
FDA UDI
Class IIActive
UD Implant System SDTH6357
FDA UDI
Class IIActive
UD Implant System SDTH4557M
FDA UDI
Class IIActive
UD Implant System UDH4545M
FDA UDI
Class IIActive
Chaorum Implant System MSIPH45S
FDA UDI
Class IActive
UD Implant System SBA3525M
FDA UDI
Class IIActive
UD Implant System SDTH6154
FDA UDI
Class IIActive
Chaorum Implant System MSDH60454
FDA UDI
Class IIActive
Chaorum Implant System MSF3013M
FDA UDI
Class IIActive
UD Implant System UDH4015
FDA UDI
Class IIActive
UD Implant System UDS5007M
FDA UDI
Class IIActive
Chaorum Implant System MDH7545
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65357
FDA UDI
Class IIActive
UD Implant System UAAN45253
FDA UDI
Class IIActive
Chaorum Implant System MSAA40174M
FDA UDI
Class IIActive
UD Implant System SDTN6157
FDA UDI
Class IIActive
Chaorum Implant System MSDN50554
FDA UDI
Class IIActive
Chaorum Implant System MSDH60255
FDA UDI
Class IIActive
UD Implant System UDS4507M
FDA UDI
Class IIActive
Chaorum Implant System SFBR4514
FDA UDI
Class IIActive
Chaorum Implant System MSMA4525N
FDA UDI
Class IIActive
Chaorum Implant System MDH3535M
FDA UDI
Class IIActive
Chaorum Implant System STA3520MN
FDA UDI
Class IIActive
Chaorum Implant System MSCA4525
FDA UDI
Class IIActive
Chaorum Implant System CSAA60173
FDA UDI
Class IIActive
Chaorum Implant System STA4010MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA45175N
FDA UDI
Class IIActive
Chaorum Implant System MSCA4055M
FDA UDI
Class IIActive
Chaorum Implant System MSDN55157
FDA UDI
Class IIActive
UD Implant System UDH6500
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50457
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