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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
—
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 1 of 35
DeviceModel / ReferenceRegistriesClassStatus
UD Implant System UDH6525
FDA UDI
Class IIActive
Chaorum Implant System MSCAS5010
FDA UDI
Class IIActive
Chaorum Implant System SFBR4014
FDA UDI
Class IIActive
Chaorum Implant System MSCA4515M
FDA UDI
Class IIActive
Chaorum Implant System MDH4555
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60104
FDA UDI
Class IIActive
Chaorum Implant System MSDH65254
FDA UDI
Class IIActive
Chaorum Implant System MSMA4010MH
FDA UDI
Class IIActive
Chaorum Implant System MSF5007
FDA UDI
Class IIActive
Chaorum Implant System MSMA5025H
FDA UDI
Class IIActive
Chaorum Implant System CSAA60155N
FDA UDI
Class IIActive
Chaorum Implant System MSMA4035MN
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50157
FDA UDI
Class IIActive
UD Implant System SDTN6557
FDA UDI
Class IIActive
Chaorum Implant System MSMA4055MH
FDA UDI
Class IIActive
Chaorum Implant System MSMA4515MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN45355
FDA UDI
Class IIActive
Chaorum Implant System MSMA4525H
FDA UDI
Class IIActive
Chaorum Implant System CSAA55251N
FDA UDI
Class IIActive
Chaorum Implant System CSAA60252
FDA UDI
Class IIActive
Chaorum Implant System MSCAS3510M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40175M
FDA UDI
Class IIActive
UD Implant System UAAH45154M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60557
FDA UDI
Class IIActive
Chaorum Implant System SFBR4510
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50557
FDA UDI
Class IIActive
UD Implant System MSTA4010MH
FDA UDI
Class IIActive
Chaorum Implant System MSDN50107
FDA UDI
Class IIActive
Chaorum Implant System MSMA5530H
FDA UDI
Class IIActive
UD Implant System SDTH4257
FDA UDI
Class IIActive
Chaorum Implant System CSAA55254
FDA UDI
Class IIActive
Chaorum Implant System PSFR4515S
FDA UDI
Class IIActive
Chaorum Implant System ATFS3010M
FDA UDI
Class IIActive
Chaorum Implant System MSF6015
FDA UDI
Class IIActive
Chaorum Implant System MSDH55557
FDA UDI
Class IIActive
Chaorum Implant System MSMA4520H
FDA UDI
Class IIActive
Chaorum Implant System MSCA5535
FDA UDI
Class IIActive
Chaorum Implant System MDH6545
FDA UDI
Class IIActive
Chaorum Implant System STA3540MN
FDA UDI
Class IIActive
Chaorum Implant System ASFS3008M
FDA UDI
Class IIActive
UD Implant System UAAH45251M
FDA UDI
Class IIActive
Chaorum Implant System PSFS3013MS
FDA UDI
Class IIActive
Chaorum Implant System CSAA40175M
FDA UDI
Class IIActive
Chaorum Implant System MSDH45257M
FDA UDI
Class IIActive
Chaorum Implant System CSAA55172
FDA UDI
Class IIActive
UD Implant System MSCSM12
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3012M
FDA UDI
Class IIActive
Chaorum Implant System STA5555N
FDA UDI
Class IIActive
Chaorum Implant System MSF3010M
FDA UDI
Class IIActive
Chaorum Implant System STA5535N
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