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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 15 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System STA4020MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH35255M
FDA UDI
Class IIActive
Chaorum Implant System MDH4535M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40357M
FDA UDI
Class IIActive
UD Implant System SDTH425M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40554M
FDA UDI
Class IIActive
UD Implant System SDTN6154
FDA UDI
Class IIActive
Chaorum Implant System ASFS3012MS
FDA UDI
Class IIActive
Chaorum Implant System ATFW6008S
FDA UDI
Class IIActive
Chaorum Implant System MSAA45155
FDA UDI
Class IIActive
UD Implant System UDH6515
FDA UDI
Class IIActive
Chaorum Implant System ASFR4512
FDA UDI
Class IIActive
Chaorum Implant System MSDH60155
FDA UDI
Class IIActive
Chaorum Implant System MSMA6040H
FDA UDI
Class IIActive
Chaorum Implant System MSDH55355
FDA UDI
Class IIActive
Chaorum Implant System SFBW6008
FDA UDI
Class IIActive
Chaorum Implant System MSDN60457
FDA UDI
Class IIActive
Chaorum Implant System MSDH60104
FDA UDI
Class IIActive
UD Implant System UAAH45253M
FDA UDI
Class IIActive
Chaorum Implant System MDH5535
FDA UDI
Class IIActive
Chaorum Implant System MSBA3555M
FDA UDI
Class IIActive
UD Implant System SDTH415M
FDA UDI
Class IIActive
UD Implant System SDTN510
FDA UDI
Class IIActive
Chaorum Implant System MSAA45155N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45557M
FDA UDI
Class IIActive
Chaorum Implant System MSDN60157
FDA UDI
Class IIActive
UD Implant System SCTT625
FDA UDI
Class IIActive
UD Implant System SDTN4254
FDA UDI
Class IIActive
UD Implant System SDTH5254
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45357
FDA UDI
Class IIActive
UD Implant System MSTA4510H
FDA UDI
Class IIActive
Chaorum Implant System MSDH50557
FDA UDI
Class IIActive
Chaorum Implant System STA4555N
FDA UDI
Class IIActive
Chaorum Implant System STA5550H
FDA UDI
Class IIActive
Chaorum Implant System CSAA45173N
FDA UDI
Class IIActive
Chaorum Implant System STA4010MH
FDA UDI
Class IIActive
Chaorum Implant System MDH5045
FDA UDI
Class IIActive
Chaorum Implant System PSFW5010
FDA UDI
Class IIActive
Chaorum Implant System MSDN35454M
FDA UDI
Class IIActive
Chaorum Implant System ASFR4512S
FDA UDI
Class IIActive
Chaorum Implant System MSDH50104
FDA UDI
Class IIActive
Chaorum Implant System PSFS3011M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60455
FDA UDI
Class IIActive
UD Implant System SCTT4025M
FDA UDI
Class IIActive
Chaorum Implant System ASFW6010
FDA UDI
Class IIActive
Chaorum Implant System ATFS3012MS
FDA UDI
Class IIActive
UD Implant System SCTT635
FDA UDI
Class IIActive
Chaorum Implant System MSAA40173M
FDA UDI
Class IIActive
Chaorum Implant System MSDN55455
FDA UDI
Class IIActive
Chaorum Implant System MSDH45555M
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