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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
—
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 5 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System ATFW6008
FDA UDI
Class IIActive
Chaorum Implant System CSAA60174
FDA UDI
Class IIActive
Chaorum Implant System STA4055MH
FDA UDI
Class IIActive
Chaorum Implant System MDH8515
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50154
FDA UDI
Class IIActive
Chaorum Implant System MSAA40253M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45152N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS35354M
FDA UDI
Class IIActive
Chaorum Implant System MSDN45155M
FDA UDI
Class IIActive
UD Implant System SCTT445
FDA UDI
Class IIActive
UD Implant System UDH6510
FDA UDI
Class IIActive
Chaorum Implant System STA4515MH
FDA UDI
Class IIActive
Chaorum Implant System ATFR4008
FDA UDI
Class IIActive
Chaorum Implant System MDH4035
FDA UDI
Class IIActive
Chaorum Implant System MSAA55252N
FDA UDI
Class IIActive
UD Implant System UDH4555M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40254M
FDA UDI
Class IIActive
UD Implant System SCTT555
FDA UDI
Class IIActive
UD Implant System SDTN6104
FDA UDI
Class IIActive
Chaorum Implant System MSDN35104M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40152M
FDA UDI
Class IIActive
Chaorum Implant System MSAA50152N
FDA UDI
Class IIActive
UD Implant System UDS5011M
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3014M
FDA UDI
Class IIActive
UD Implant System UAAN45153M
FDA UDI
Class IIActive
Chaorum Implant System MSAA60255
FDA UDI
Class IIActive
Chaorum Implant System CSAA40173MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN55557
FDA UDI
Class IIActive
Chaorum Implant System MSMA4555MH
FDA UDI
Class IIActive
Chaorum Implant System MSAA45252MN
FDA UDI
Class IIActive
UD Implant System SMA4520H
FDA UDI
Class IIActive
Chaorum Implant System MSAA35153M
FDA UDI
Class IIActive
Chaorum Implant System CSAA40174M
FDA UDI
Class IIActive
Chaorum Implant System MDH4510M
FDA UDI
Class IIActive
UD Implant System SCTT645
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45254M
FDA UDI
Class IIActive
UD Implant System SDTH4457
FDA UDI
Class IIActive
Chaorum Implant System MSCAS6015
FDA UDI
Class IIActive
Chaorum Implant System MSMA6025N
FDA UDI
Class IIActive
Chaorum Implant System MSDN55104
FDA UDI
Class IIActive
Chaorum Implant System ASFS3608MS
FDA UDI
Class IIActive
Chaorum Implant System MSMA6515H
FDA UDI
Class IIActive
Chaorum Implant System MSAA40155MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA45252N
FDA UDI
Class IIActive
Chaorum Implant System MSAA35155M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55107
FDA UDI
Class IIActive
UD Implant System SCTT435M
FDA UDI
Class IIActive
Chaorum Implant System MSBA4040
FDA UDI
Class IIActive
Chaorum Implant System CSAA60173N
FDA UDI
Class IIActive
Chaorum Implant System MSDN60105
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