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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
—
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 7 of 35
DeviceModel / ReferenceRegistriesClassStatus
UD Implant System SCTT410
FDA UDI
Class IIActive
Chaorum Implant System MSBA3530
FDA UDI
Class IIActive
Chaorum Implant System ATFS3010MS
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3610
FDA UDI
Class IIActive
Chaorum Implant System MSDN60454
FDA UDI
Class IIActive
Chaorum Implant System MSMA6525N
FDA UDI
Class IIActive
Chaorum Implant System MSCA4510M
FDA UDI
Class IIActive
Chaorum Implant System MDH4545
FDA UDI
Class IIActive
Chaorum Implant System CSAA40151M
FDA UDI
Class IIActive
Chaorum Implant System ATFR4010
FDA UDI
Class IIActive
Chaorum Implant System MSAA55254N
FDA UDI
Class IIActive
UD Implant System SDTH5454
FDA UDI
Class IIActive
Chaorum Implant System PSFR4008S
FDA UDI
Class IIActive
Chaorum Implant System MSDN45354M
FDA UDI
Class IIActive
Chaorum Implant System MSMA5525N
FDA UDI
Class IIActive
UD Implant System UAAH55153
FDA UDI
Class IIActive
Chaorum Implant System MSDH35455M
FDA UDI
Class IIActive
UD Implant System UDS6008M
FDA UDI
Class IIActive
Chaorum Implant System STA4050MH
FDA UDI
Class IIActive
Chaorum Implant System STA5015N
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4014
FDA UDI
Class IIActive
Chaorum Implant System PSFS3510MS
FDA UDI
Class IIActive
Chaorum Implant System MSAA40254MN
FDA UDI
Class IIActive
Chaorum Implant System ATFS3608
FDA UDI
Class IIActive
Chaorum Implant System ATFS3008M
FDA UDI
Class IIActive
Chaorum Implant System MSCA4510
FDA UDI
Class IIActive
Chaorum Implant System CSAA45254MN
FDA UDI
Class IIActive
Chaorum Implant System MSAA50252N
FDA UDI
Class IIActive
Chaorum Implant System CSAA50155
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3612M
FDA UDI
Class IIActive
Chaorum Implant System SFBW6012
FDA UDI
Class IIActive
UD Implant System SDTH40107M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60253N
FDA UDI
Class IIActive
Chaorum Implant System PSFW5011
FDA UDI
Class IIActive
Chaorum Implant System PSFW6011S
FDA UDI
Class IIActive
Chaorum Implant System ATFS3612S
FDA UDI
Class IIActive
UD Implant System SDTH4157
FDA UDI
Class IIActive
Chaorum Implant System MDH5545
FDA UDI
Class IIActive
Chaorum Implant System ATFR4512
FDA UDI
Class IIActive
UD Implant System SDTN655
FDA UDI
Class IIActive
Chaorum Implant System STA4050MN
FDA UDI
Class IIActive
Chaorum Implant System ATFS3014MS
FDA UDI
Class IIActive
Chaorum Implant System PSFS3010M
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4508
FDA UDI
Class IIActive
Chaorum Implant System PSFS3015M
FDA UDI
Class IIActive
Chaorum Implant System MDH4045M
FDA UDI
Class IIActive
UD Implant System UAAN45151M
FDA UDI
Class IIActive
Chaorum Implant System STA4535N
FDA UDI
Class IIActive
Chaorum Implant System MSMA4510N
FDA UDI
Class IIActive
UD Implant System SDTN455M
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