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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 29 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSDH35105M
FDA UDI
Class IIActive
Chaorum Implant System MSCA6515
FDA UDI
Class IIActive
Chaorum Implant System MSAA45151MN
FDA UDI
Class IIActive
Chaorum Implant System MDH5015
FDA UDI
Class IIActive
Chaorum Implant System CSAA45172
FDA UDI
Class IIActive
Chaorum Implant System MSDH40157M
FDA UDI
Class IIActive
Chaorum Implant System ASFS3610
FDA UDI
Class IIActive
UD Implant System SDTN4557
FDA UDI
Class IIActive
Chaorum Implant System ASFW5010S
FDA UDI
Class IIActive
Chaorum Implant System ASFR4008S
FDA UDI
Class IIActive
Chaorum Implant System MSDN35154M
FDA UDI
Class IIActive
Chaorum Implant System MPUMN
FDA UDI
Class IActive
Chaorum Implant System MSITH45S
FDA UDI
Class IActive
Chaorum Implant System MSMA4535MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH40107M
FDA UDI
Class IIActive
Chaorum Implant System MDH4010M
FDA UDI
Class IIActive
Chaorum Implant System MSDN65457
FDA UDI
Class IIActive
Chaorum Implant System MSAA45155MN
FDA UDI
Class IIActive
Chaorum Implant System STA5055N
FDA UDI
Class IIActive
Chaorum Implant System MSBA3530M
FDA UDI
Class IIActive
Chaorum Implant System CSAA60254
FDA UDI
Class IIActive
Chaorum Implant System MSDH50254
FDA UDI
Class IIActive
Chaorum Implant System ATFS3015MS
FDA UDI
Class IIActive
UD Implant System SDTH415
FDA UDI
Class IIActive
Chaorum Implant System MSAA35155MN
FDA UDI
Class IIActive
Chaorum Implant System PSFW6010
FDA UDI
Class IIActive
Chaorum Implant System MSDN45357
FDA UDI
Class IIActive
Chaorum Implant System STA5510N
FDA UDI
Class IIActive
Chaorum Implant System MSDN45157M
FDA UDI
Class IIActive
Chaorum Implant System MSAA35152M
FDA UDI
Class IIActive
UD Implant System SBA3510M
FDA UDI
Class IIActive
Chaorum Implant System MSDH40557M
FDA UDI
Class IIActive
Chaorum Implant System MSMA4010MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA60171
FDA UDI
Class IIActive
Chaorum Implant System MSAA45154N
FDA UDI
Class IIActive
Chaorum Implant System PSFW5010S
FDA UDI
Class IIActive
Chaorum Implant System MSBA3520
FDA UDI
Class IIActive
Chaorum Implant System CSAA60154N
FDA UDI
Class IIActive
Chaorum Implant System MSDH50157
FDA UDI
Class IIActive
Chaorum Implant System MSDN55257
FDA UDI
Class IIActive
UD Implant System UAAN45152
FDA UDI
Class IIActive
Chaorum Implant System MSAA60253N
FDA UDI
Class IIActive
Chaorum Implant System MSMA5520N
FDA UDI
Class IIActive
Chaorum Implant System MSDN45554
FDA UDI
Class IIActive
Chaorum Implant System MDH7515
FDA UDI
Class IIActive
Chaorum Implant System MSDH35355M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45253M
FDA UDI
Class IIActive
Chaorum Implant System CSAA35152M
FDA UDI
Class IIActive
Chaorum Implant System STA4540MH
FDA UDI
Class IIActive
Chaorum Implant System MSDH40104M
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