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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 25 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MSDH50257
FDA UDI
Class IIActive
Chaorum Implant System SFBR4012
FDA UDI
Class IIActive
Chaorum Implant System MSDN45455
FDA UDI
Class IIActive
Chaorum Implant System MSDH40555M
FDA UDI
Class IIActive
Chaorum Implant System CSAA55175
FDA UDI
Class IIActive
Chaorum Implant System MSBA3525M
FDA UDI
Class IIActive
Chaorum Implant System MSDH65457
FDA UDI
Class IIActive
Chaorum Implant System STA4020MN
FDA UDI
Class IIActive
Chaorum Implant System MSMA4015N
FDA UDI
Class IIActive
Chaorum Implant System MSDH55455
FDA UDI
Class IIActive
Chaorum Implant System MSDH45107
FDA UDI
Class IIActive
Chaorum Implant System MSDN55254
FDA UDI
Class IIActive
Chaorum Implant System MSDH65155
FDA UDI
Class IIActive
Chaorum Implant System MSAA40255MN
FDA UDI
Class IIActive
Chaorum Implant System MSF5008
FDA UDI
Class IIActive
Chaorum Implant System MSAA45252
FDA UDI
Class IIActive
UD Implant System SDTH4554
FDA UDI
Class IIActive
Chaorum Implant System STA4030MN
FDA UDI
Class IIActive
Chaorum Implant System PSFR4511
FDA UDI
Class IIActive
Chaorum Implant System STA5545H
FDA UDI
Class IIActive
Chaorum Implant System CSAA50154N
FDA UDI
Class IIActive
Chaorum Implant System CSAA55251
FDA UDI
Class IIActive
Chaorum Implant System MSBA4020
FDA UDI
Class IIActive
Chaorum Implant System STA5555H
FDA UDI
Class IIActive
UD Implant System SCTT4010M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS35454M
FDA UDI
Class IIActive
UD Implant System SDTN4025M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40157M
FDA UDI
Class IIActive
UD Implant System UAAH45251
FDA UDI
Class IIActive
Chaorum Implant System MDH4525
FDA UDI
Class IIActive
Chaorum Implant System MSCAS50454
FDA UDI
Class IIActive
UD Implant System SDTH4035M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60355
FDA UDI
Class IIActive
UD Implant System UDH4000
FDA UDI
Class IIActive
Chaorum Implant System MSDN65354
FDA UDI
Class IIActive
Chaorum Implant System MSDH45354
FDA UDI
Class IIActive
UD Implant System SCTT4055M
FDA UDI
Class IIActive
UD Implant System SBA3525
FDA UDI
Class IIActive
UD Implant System UDS4011M
FDA UDI
Class IIActive
Chaorum Implant System MSDN40254M
FDA UDI
Class IIActive
UD Implant System SDTN4107M
FDA UDI
Class IIActive
Chaorum Implant System MSMA3515MN
FDA UDI
Class IIActive
Chaorum Implant System PSFR4508
FDA UDI
Class IIActive
UD Implant System SDTN645
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45104
FDA UDI
Class IIActive
Chaorum Implant System MSF4507
FDA UDI
Class IIActive
Chaorum Implant System MSCA35354M
FDA UDI
Class IIActive
UD Implant System UAAH45254
FDA UDI
Class IIActive
Chaorum Implant System CSAA45173
FDA UDI
Class IIActive
UD Implant System SDTH6557
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