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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 32 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System CSAA35151MN
FDA UDI
Class IIActive
Chaorum Implant System ATFR4508
FDA UDI
Class IIActive
Chaorum Implant System CSAA60172
FDA UDI
Class IIActive
Chaorum Implant System MSDN45104
FDA UDI
Class IIActive
Chaorum Implant System MSMA3555MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA45175MN
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45107
FDA UDI
Class IIActive
Chaorum Implant System MSCA4010M
FDA UDI
Class IIActive
Chaorum Implant System CSAA55253
FDA UDI
Class IIActive
Chaorum Implant System ATFW6012
FDA UDI
Class IIActive
Chaorum Implant System MSMA6535H
FDA UDI
Class IIActive
Chaorum Implant System MSMA4025MH
FDA UDI
Class IIActive
Chaorum Implant System MSAA45151N
FDA UDI
Class IIActive
Chaorum Implant System MSDN45555
FDA UDI
Class IIActive
Chaorum Implant System MSAA45254N
FDA UDI
Class IIActive
Chaorum Implant System MSDH40357M
FDA UDI
Class IIActive
Chaorum Implant System STA4530N
FDA UDI
Class IIActive
Chaorum Implant System MSAA50153
FDA UDI
Class IIActive
Chaorum Implant System CSAA40153MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA55253
FDA UDI
Class IIActive
Chaorum Implant System MSMA3510MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH35254M
FDA UDI
Class IIActive
Chaorum Implant System ATFR4014
FDA UDI
Class IIActive
Chaorum Implant System MSLAM
FDA UDI
Class IActive
Chaorum Implant System MSBA3520M
FDA UDI
Class IIActive
Chaorum Implant System ATFR4514
FDA UDI
Class IIActive
Chaorum Implant System MSDN35254M
FDA UDI
Class IIActive
Chaorum Implant System ATFW5010
FDA UDI
Class IIActive
UD Implant System UAAN45253M
FDA UDI
Class IIActive
Chaorum Implant System STA4040MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN55354
FDA UDI
Class IIActive
Chaorum Implant System MSAA45151M
FDA UDI
Class IIActive
UD Implant System UDS6007M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50455
FDA UDI
Class IIActive
Chaorum Implant System MSDH60154
FDA UDI
Class IIActive
UD Implant System SCTT655
FDA UDI
Class IIActive
Chaorum Implant System MSDH45355M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40171M
FDA UDI
Class IIActive
UD Implant System UDS3508M
FDA UDI
Class IIActive
UD Implant System UDH4055M
FDA UDI
Class IIActive
Chaorum Implant System MSMA3545MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA50174
FDA UDI
Class IIActive
UD Implant System SCTT4035M
FDA UDI
Class IIActive
UD Implant System UDH4515
FDA UDI
Class IIActive
Chaorum Implant System PSFR4010
FDA UDI
Class IIActive
UD Implant System UDH4015M
FDA UDI
Class IIActive
Chaorum Implant System PSFR4508S
FDA UDI
Class IIActive
Chaorum Implant System ASFBW6012
FDA UDI
Class IIActive
Chaorum Implant System STA5535H
FDA UDI
Class IIActive
UD Implant System UAAN45254M
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