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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 31 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System PSFS3511MS
FDA UDI
Class IIActive
Chaorum Implant System CSAA55154N
FDA UDI
Class IIActive
Chaorum Implant System CSAA40152MN
FDA UDI
Class IIActive
Chaorum Implant System MSF4013
FDA UDI
Class IIActive
Chaorum Implant System STA4525N
FDA UDI
Class IIActive
Chaorum Implant System STA5530N
FDA UDI
Class IIActive
Chaorum Implant System CSAA45252N
FDA UDI
Class IIActive
Chaorum Implant System MSDN40455M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45171MN
FDA UDI
Class IIActive
UD Implant System UAAN55154
FDA UDI
Class IIActive
Chaorum Implant System CSAA60153
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45257
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65154
FDA UDI
Class IIActive
Chaorum Implant System MSCAS3525M
FDA UDI
Class IIActive
Chaorum Implant System MSDH45355
FDA UDI
Class IIActive
UD Implant System SDTN555
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45154M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45254
FDA UDI
Class IIActive
UD Implant System SCTT525
FDA UDI
Class IIActive
UD Implant System SDTN5354
FDA UDI
Class IIActive
Chaorum Implant System MSDH40105M
FDA UDI
Class IIActive
UD Implant System SDTN4554
FDA UDI
Class IIActive
Chaorum Implant System MSAA45155M
FDA UDI
Class IIActive
Chaorum Implant System MSDN60155
FDA UDI
Class IIActive
Chaorum Implant System MSBA3510M
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4008
FDA UDI
Class IIActive
Chaorum Implant System CSAA60151
FDA UDI
Class IIActive
Chaorum Implant System MSMA6010N
FDA UDI
Class IIActive
Chaorum Implant System CSAA45154M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45172MN
FDA UDI
Class IIActive
Chaorum Implant System MDH4025
FDA UDI
Class IIActive
UD Implant System UAAN45251M
FDA UDI
Class IIActive
UD Implant System MSTA4510N
FDA UDI
Class IIActive
Chaorum Implant System MSDN55454
FDA UDI
Class IIActive
Chaorum Implant System MSAA45154M
FDA UDI
Class IIActive
Chaorum Implant System MSCA4555
FDA UDI
Class IIActive
Chaorum Implant System MSAA40154MN
FDA UDI
Class IIActive
Chaorum Implant System PSFW6008
FDA UDI
Class IIActive
Chaorum Implant System MSDN50255
FDA UDI
Class IIActive
UD Implant System UDH4045
FDA UDI
Class IIActive
Chaorum Implant System CSAA35155MN
FDA UDI
Class IIActive
Chaorum Implant System SFBW5010
FDA UDI
Class IIActive
Chaorum Implant System MSAA45254
FDA UDI
Class IIActive
Chaorum Implant System MSMA4530H
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4012
FDA UDI
Class IIActive
Chaorum Implant System MSDN45555M
FDA UDI
Class IIActive
UD Implant System UAAH45252M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45174M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50154
FDA UDI
Class IIActive
Chaorum Implant System MSAA55254
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