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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 33 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MDH6510
FDA UDI
Class IIActive
UD Implant System SDTH6104
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40454M
FDA UDI
Class IIActive
Chaorum Implant System MSAA40153M
FDA UDI
Class IIActive
UD Implant System SDTN5454
FDA UDI
Class IIActive
UD Implant System SDTN4457
FDA UDI
Class IIActive
Chaorum Implant System CSAA40252MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN55554
FDA UDI
Class IIActive
UD Implant System SDTN4045M
FDA UDI
Class IIActive
UD Implant System SDTH40157M
FDA UDI
Class IIActive
Chaorum Implant System CSAA45151MN
FDA UDI
Class IIActive
Chaorum Implant System MSMA3535MH
FDA UDI
Class IIActive
Chaorum Implant System MSMA4545MN
FDA UDI
Class IIActive
Chaorum Implant System PSFW6011
FDA UDI
Class IIActive
Chaorum Implant System CSAA55175N
FDA UDI
Class IIActive
Chaorum Implant System ASFS3614MS
FDA UDI
Class IIActive
Chaorum Implant System STA3535MN
FDA UDI
Class IIActive
Chaorum Implant System ASFS3015MS
FDA UDI
Class IIActive
Chaorum Implant System STA5035H
FDA UDI
Class IIActive
Chaorum Implant System ASFBW5012
FDA UDI
Class IIActive
Chaorum Implant System MSDH50457
FDA UDI
Class IIActive
Chaorum Implant System ATFR4514S
FDA UDI
Class IIActive
Chaorum Implant System MSAA40253MN
FDA UDI
Class IIActive
Chaorum Implant System CSAA50253
FDA UDI
Class IIActive
Chaorum Implant System MSAA50255N
FDA UDI
Class IIActive
Chaorum Implant System CSAA40172M
FDA UDI
Class IIActive
Chaorum Implant System MSAA60152N
FDA UDI
Class IIActive
Chaorum Implant System ASFW5008S
FDA UDI
Class IIActive
Chaorum Implant System PSFR4010S
FDA UDI
Class IIActive
UD Implant System UAAN55251
FDA UDI
Class IIActive
Chaorum Implant System PSFS3508M
FDA UDI
Class IIActive
Chaorum Implant System SFBS3010M
FDA UDI
Class IIActive
Chaorum Implant System PSFW5013
FDA UDI
Class IIActive
Chaorum Implant System MDH7535
FDA UDI
Class IIActive
Chaorum Implant System ASFBW6010
FDA UDI
Class IIActive
Chaorum Implant System MDH4555M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3008MS
FDA UDI
Class IIActive
Chaorum Implant System STA3510MH
FDA UDI
Class IIActive
Chaorum Implant System CSAA50154
FDA UDI
Class IIActive
Chaorum Implant System MSAA40254M
FDA UDI
Class IIActive
Chaorum Implant System MSDH55107
FDA UDI
Class IIActive
Chaorum Implant System MSDN65557
FDA UDI
Class IIActive
Chaorum Implant System MDH6025
FDA UDI
Class IIActive
Chaorum Implant System CSAA55171N
FDA UDI
Class IIActive
Chaorum Implant System MSMA5030H
FDA UDI
Class IIActive
Chaorum Implant System CSAA60152N
FDA UDI
Class IIActive
Chaorum Implant System MSCAS45554M
FDA UDI
Class IIActive
UD Implant System SCTT455M
FDA UDI
Class IIActive
UD Implant System UDH4010
FDA UDI
Class IIActive
Chaorum Implant System MSDH45104
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