Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
557812771

Catalogue (1719)

Page 23 of 35
DeviceModel / ReferenceRegistriesClassStatus
Chaorum Implant System MDH5525
FDA UDI
Class IIActive
Chaorum Implant System MSCAS60257
FDA UDI
Class IIActive
Chaorum Implant System CSAA55254N
FDA UDI
Class IIActive
Chaorum Implant System CSAA50173
FDA UDI
Class IIActive
Chaorum Implant System PSFR4511S
FDA UDI
Class IIActive
Chaorum Implant System STA5030H
FDA UDI
Class IIActive
Chaorum Implant System MSMA4015MH
FDA UDI
Class IIActive
Chaorum Implant System MSCAS65104
FDA UDI
Class IIActive
Chaorum Implant System MSAA45253
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55257
FDA UDI
Class IIActive
UD Implant System SDTN4154
FDA UDI
Class IIActive
Chaorum Implant System MSDN55105
FDA UDI
Class IIActive
UD Implant System SDTN4104
FDA UDI
Class IIActive
Chaorum Implant System SFBW5014
FDA UDI
Class IIActive
Chaorum Implant System MSDH55555
FDA UDI
Class IIActive
Chaorum Implant System MSAA45172MN
FDA UDI
Class IIActive
Chaorum Implant System PSFW5008
FDA UDI
Class IIActive
Chaorum Implant System STA3515MN
FDA UDI
Class IIActive
Chaorum Implant System MSMA4015H
FDA UDI
Class IIActive
Chaorum Implant System MSDN45554M
FDA UDI
Class IIActive
Chaorum Implant System MSBA4050M
FDA UDI
Class IIActive
Chaorum Implant System MSAA45174MN
FDA UDI
Class IIActive
Chaorum Implant System STA4035MN
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40557M
FDA UDI
Class IIActive
Chaorum Implant System MSDN40155M
FDA UDI
Class IIActive
Chaorum Implant System MSF4007
FDA UDI
Class IIActive
Chaorum Implant System MSMA3545MH
FDA UDI
Class IIActive
Chaorum Implant System MSDN35255M
FDA UDI
Class IIActive
UD Implant System SDTH5257
FDA UDI
Class IIActive
Chaorum Implant System MSMA5515N
FDA UDI
Class IIActive
Chaorum Implant System SFBS3008M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3610S
FDA UDI
Class IIActive
Chaorum Implant System ASFS3014M
FDA UDI
Class IIActive
Chaorum Implant System MSAA55153N
FDA UDI
Class IIActive
Chaorum Implant System ATFW6012S
FDA UDI
Class IIActive
Chaorum Implant System MSDN40557M
FDA UDI
Class IIActive
UD Implant System SDTN6554
FDA UDI
Class IIActive
Chaorum Implant System CSAA60154
FDA UDI
Class IIActive
Chaorum Implant System MSDH40257M
FDA UDI
Class IIActive
Chaorum Implant System MDH3510M
FDA UDI
Class IIActive
Chaorum Implant System PSFW5015S
FDA UDI
Class IIActive
Chaorum Implant System CSAA50175
FDA UDI
Class IIActive
Chaorum Implant System MSCA4045M
FDA UDI
Class IIActive
Chaorum Implant System MDH4055
FDA UDI
Class IIActive
Chaorum Implant System MSDH55157
FDA UDI
Class IIActive
Chaorum Implant System MSAA50151N
FDA UDI
Class IIActive
UD Implant System UAAN45154M
FDA UDI
Class IIActive
Chaorum Implant System MSDN50105
FDA UDI
Class IIActive
Chaorum Implant System MSBA3535
FDA UDI
Class IIActive
UD Implant System SDTH6554
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Medimecca Co Ltd Seoul · KR FEI 3007649394