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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
—
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 11 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSCAS6010
FDA UDI
Class IIActive
Chaorum Implant System MSDH45557M
FDA UDI
Class IIActive
UD Implant System UDS4511M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3012M
FDA UDI
Class IIActive
Chaorum Implant System ASFS3610MS
FDA UDI
Class IIActive
Chaorum Implant System MSAA40173MN
FDA UDI
Class IIActive
Chaorum Implant System MSCA4515
FDA UDI
Class IIActive
UD Implant System UDS4008M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60254
FDA UDI
Class IIActive
Chaorum Implant System MSAA35152MN
FDA UDI
Class IIActive
Chaorum Implant System STA4545MN
FDA UDI
Class IIActive
Chaorum Implant System SFBS3015M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45255
FDA UDI
Class IIActive
UD Implant System UDH4010M
FDA UDI
Class IIActive
Chaorum Implant System MSCA6535
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45354M
FDA UDI
Class IIActive
Chaorum Implant System MSDN60455
FDA UDI
Class IIActive
UD Implant System SCTT515
FDA UDI
Class IIActive
Chaorum Implant System MSAA45153N
FDA UDI
Class IIActive
UD Implant System SMA6525N
FDA UDI
Class IIActive
Chaorum Implant System MDH4515
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3085M
FDA UDI
Class IIActive
Chaorum Implant System MSDN60354
FDA UDI
Class IIActive
UD Implant System UDH5535
FDA UDI
Class IIActive
Chaorum Implant System CSAA50151N
FDA UDI
Class IIActive
UD Implant System UDS5010M
FDA UDI
Class IIActive
Chaorum Implant System STA4555MH
FDA UDI
Class IIActive
Chaorum Implant System MSMA6535N
FDA UDI
Class IIActive
Chaorum Implant System MSBA3525
FDA UDI
Class IIActive
Chaorum Implant System MSMA6035H
FDA UDI
Class IIActive
Chaorum Implant System STA5055H
FDA UDI
Class IIActive
Chaorum Implant System MDH4015M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60254N
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3008M
FDA UDI
Class IIActive
Chaorum Implant System ATFW5014S
FDA UDI
Class IIActive
Chaorum Implant System SFBW5008
FDA UDI
Class IIActive
Chaorum Implant System MSBA3545M
FDA UDI
Class IIActive
Chaorum Implant System MSMA4520N
FDA UDI
Class IIActive
Chaorum Implant System MSDN50354
FDA UDI
Class IIActive
UD Implant System SMA6525H
FDA UDI
Class IIActive
UD Implant System SDTN6107
FDA UDI
Class IIActive
UD Implant System UAAH55154
FDA UDI
Class IIActive
Chaorum Implant System CSAA55151
FDA UDI
Class IIActive
Chaorum Implant System MSBA4025M
FDA UDI
Class IIActive
Chaorum Implant System MSDH50255
FDA UDI
Class IIActive
Chaorum Implant System MSDH60457
FDA UDI
Class IIActive
Chaorum Implant System ASFS3085M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40172M
FDA UDI
Class IIActive
Chaorum Implant System SFBW5012
FDA UDI
Class IIActive
Chaorum Implant System MSDH45455M
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