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 6 of 35
DeviceModel / ReferenceRegistriesClassStatus
UD Implant System SDTH610
FDA UDI
Class IIActive
Chaorum Implant System MSCA5515
FDA UDI
Class IIActive
Chaorum Implant System MSCAS40154M
FDA UDI
Class IIActive
UD Implant System UDH4035M
FDA UDI
Class IIActive
Chaorum Implant System MSDN40554M
FDA UDI
Class IIActive
Chaorum Implant System ATFS3085M
FDA UDI
Class IIActive
Chaorum Implant System MDH3545M
FDA UDI
Class IIActive
Chaorum Implant System STA5035N
FDA UDI
Class IIActive
Chaorum Implant System ASFBR4514
FDA UDI
Class IIActive
Chaorum Implant System MDH4545M
FDA UDI
Class IIActive
Chaorum Implant System CSAA35153MN
FDA UDI
Class IIActive
UD Implant System SCTT410M
FDA UDI
Class IIActive
Chaorum Implant System ASFR4008
FDA UDI
Class IIActive
Chaorum Implant System CSAA45255N
FDA UDI
Class IIActive
Chaorum Implant System MSAA45152
FDA UDI
Class IIActive
Chaorum Implant System PSFS3011MS
FDA UDI
Class IIActive
Chaorum Implant System MSAA45253MN
FDA UDI
Class IIActive
Chaorum Implant System ASFW5010
FDA UDI
Class IIActive
Chaorum Implant System ASFW5012
FDA UDI
Class IIActive
Chaorum Implant System MSF6011
FDA UDI
Class IIActive
UD Implant System SDTH4055M
FDA UDI
Class IIActive
Chaorum Implant System MSDH50155
FDA UDI
Class IIActive
Chaorum Implant System MSAA50155
FDA UDI
Class IIActive
Chaorum Implant System STA4550MN
FDA UDI
Class IIActive
Chaorum Implant System MSDN60254
FDA UDI
Class IIActive
Chaorum Implant System CSAA45255M
FDA UDI
Class IIActive
Chaorum Implant System MSCAS55104
FDA UDI
Class IIActive
UD Implant System UAAH55151
FDA UDI
Class IIActive
UD Implant System SDTH435
FDA UDI
Class IIActive
Chaorum Implant System MSDH65255
FDA UDI
Class IIActive
Chaorum Implant System MSAA40152MN
FDA UDI
Class IIActive
UD Implant System UAAN55152
FDA UDI
Class IIActive
Chaorum Implant System CSAA45255
FDA UDI
Class IIActive
Chaorum Implant System CSAA50255
FDA UDI
Class IIActive
Chaorum Implant System STA4515N
FDA UDI
Class IIActive
Chaorum Implant System MDH3515M
FDA UDI
Class IIActive
Chaorum Implant System MSBA4035M
FDA UDI
Class IIActive
Chaorum Implant System MSDH60157
FDA UDI
Class IIActive
Chaorum Implant System STA5520N
FDA UDI
Class IIActive
Chaorum Implant System MDH7510
FDA UDI
Class IIActive
Chaorum Implant System ASFS3614
FDA UDI
Class IIActive
UD Implant System UDS6013M
FDA UDI
Class IIActive
UD Implant System SCTT425
FDA UDI
Class IIActive
UD Implant System SDTN4354
FDA UDI
Class IIActive
UD Implant System UDH5555
FDA UDI
Class IIActive
Chaorum Implant System MDH4055M
FDA UDI
Class IIActive
Chaorum Implant System MSDN55357
FDA UDI
Class IIActive
Chaorum Implant System MDH6035
FDA UDI
Class IIActive
UD Implant System SDTN435
FDA UDI
Class IIActive
Chaorum Implant System ASFBS3608M
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