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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 24 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSF5010
FDA UDI
Class IIActive
Chaorum Implant System MSDN40107M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40251M
FDA UDI
Class IIActive
Chaorum Implant System CSAA50151
FDA UDI
Class IIActive
Chaorum Implant System CSAA45155MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA55253N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60154
FDA UDI
Class IIActive
Chaorum Implant System CSAA35152MN
FDA UDI
Class IIActive
UD Implant System SDTN6354
FDA UDI
Class IIActive
Chaorum Implant System CSAA40153M
FDA UDI
Class IIActive
Chaorum Implant System MSBA4010
FDA UDI
Class IIActive
Chaorum Implant System MSCA35154M
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3612
FDA UDI
Class IIActive
Chaorum Implant System PSFS3511M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45154N
FDA UDI
Class IIActive
Chaorum Implant System ASFR4508S
FDA UDI
Class IIActive
Chaorum Implant System MSCA6510
FDA UDI
Class IIActive
Chaorum Implant System CSAA45251
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4510
FDA UDI
Class IIActive
Chaorum Implant System PSFS3513MS
FDA UDI
Class IIActive
Chaorum Implant System MSDH65107
FDA UDI
Class IIActive
Chaorum Implant System MSMA6515N
FDA UDI
Class IIActive
Chaorum Implant System MSDN60355
FDA UDI
Class IIActive
Chaorum Implant System STA3545MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA50251
FDA UDI
Class IIActive
Chaorum Implant System MSCA35104M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45251MN
FDA UDI
Class IIActive
UD Implant System SDTN455
FDA UDI
Class IIActive
Chaorum Implant System MSCAS5045
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55354
FDA UDI
Class IIActive
Chaorum Implant System MSDN65454
FDA UDI
Class IIActive
UD Implant System SDTH6257
FDA UDI
Class IIActive
Chaorum Implant System MSF4510
FDA UDI
Class IIActive
UD Implant System UAAH45151
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60554
FDA UDI
Class IIActive
UD Implant System SDTH5557
FDA UDI
Class IIActive
Chaorum Implant System PSFS3013M
FDA UDI
Class IIActive
Chaorum Implant System MSDH65154
FDA UDI
Class IIActive
Chaorum Implant System PSFR4513
FDA UDI
Class IIActive
Chaorum Implant System MSDN65254
FDA UDI
Class IIActive
UD Implant System SDTH510
FDA UDI
Class IIActive
Chaorum Implant System MDH7525
FDA UDI
Class IIActive
Chaorum Implant System ASFR4510S
FDA UDI
Class IIActive
Chaorum Implant System ASFS3014MS
FDA UDI
Class IIActive
Chaorum Implant System STA5015H
FDA UDI
Class IIActive
Chaorum Implant System CSAA45252
FDA UDI
Class IIActive
UD Implant System SDTH4457M
FDA UDI
Class IIActive
UD Implant System SDTN445M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45152N
FDA UDI
Class IIActive
Chaorum Implant System MDH4500M
FDA UDI
Class IIActive

Related Companies

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Authorities

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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