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Vatech mcis Co., Ltd

US

Last updated May 23, 2026

What Vatech mcis Co., Ltd makes

Vatech mcis Co., Ltd manufactures dental appliance fabrication materials, specializing in ceramic-based products. Their portfolio includes materials used for creating dental restorations and prosthetics, such as crowns, bridges, and inlays, designed for precision and biocompatibility in dental laboratories.

The company’s products are regulated under FDA’s classification system, with devices falling into Class I and Class II categories. These materials are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations.

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 Vatech mcis Co., Ltd primarily manufacture?

Vatech mcis Co., Ltd specializes in dental appliance fabrication materials, specifically ceramic-based products. These materials are used in dental laboratories to create dental restorations and prosthetics, such as crowns, bridges, and inlays. The focus is on precision and biocompatibility to ensure safe and effective use in dental applications.

Where is Vatech mcis Co., Ltd based?

Vatech mcis Co., Ltd is based in the United States. This location influences its regulatory compliance, particularly with U.S. medical device regulations like those enforced by the FDA.

Which regulatory registries or databases list Vatech mcis Co., Ltd’s devices?

Vatech mcis Co., Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures that each device can be traced and tracked for compliance with U.S. medical device regulations, supporting transparency and accountability in the supply chain.

How are Vatech mcis Co., Ltd’s devices classified under U.S. regulations?

Vatech mcis Co., Ltd’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.

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
688284886

Catalogue (1176)

Page 9 of 24
DeviceModel / ReferenceRegistriesClassStatus
Perfit ZR NU 20 B4SM W
FDA UDI
Class IIActive
RAYZir FS FH C14 A4M
FDA UDI
Class IIActive
Perfit ZR NP 12 C1 W
FDA UDI
Class IIActive
Perfit FS FH I12 A2
FDA UDI
Class IIActive
RAYZir FS FH C16 B1M
FDA UDI
Class IIActive
Perfit FS FH B40 B2M
FDA UDI
Class IIActive
Perfit ZR NA 22 A1 W
FDA UDI
Class IIActive
Perfit ZR NA 25 A1 W
FDA UDI
Class IIActive
Perfit ZR NU 25 B2TM W
FDA UDI
Class IIActive
Perfit ZR NP 25 C2 W
FDA UDI
Class IIActive
RAYZir FS FH C14 D2
FDA UDI
Class IIActive
Perfit ZR NU 25 C2TM W
FDA UDI
Class IIActive
RAYZir FS FH C16 A3.5
FDA UDI
Class IIActive
Perfit FS FH C14 B3
FDA UDI
Class IIActive
Perfit FS FH I10 A4M
FDA UDI
Class IIActive
Perfit ZR NU 25 C1 W
FDA UDI
Class IIActive
Perfit ZR NA 22 B3 W
FDA UDI
Class IIActive
Perfit ZR NP 12 B2 W
FDA UDI
Class IIActive
RAYZir FS FH I12 D4
FDA UDI
Class IIActive
Perfit ZR NA 22 C1 W
FDA UDI
Class IIActive
Perfit ZR NU 14 C1SM W
FDA UDI
Class IIActive
RAYZir FS FH C14 C1M
FDA UDI
Class IIActive
Perfit ZR NU 20 BL2 W
FDA UDI
Class IActive
Perfit ZR NA 10 A3 W
FDA UDI
Class IIActive
Perfit ZR NU 20 C1 W
FDA UDI
Class IIActive
Perfit ZR NA 20 A4 W
FDA UDI
Class IIActive
Perfit FS FH B32 C1
FDA UDI
Class IIActive
Perfit ZR NU 20 B3 W
FDA UDI
Class IIActive
RAYZir FS FH I12 A1
FDA UDI
Class IIActive
Perfit FS FH B32 A2
FDA UDI
Class IIActive
Perfit ZR NU 16 BL2 W
FDA UDI
Class IActive
Perfit ZR NU 25 A3.5SM W
FDA UDI
Class IIActive
Perfit ZR NP 10 A3 W
FDA UDI
Class IIActive
Perfit ZR NP 25 A4 W
FDA UDI
Class IIActive
Perfit ZR NP 22 D3 W
FDA UDI
Class IIActive
Perfit ZR NU 12 B1 W
FDA UDI
Class IIActive
Chairside Zirconia FH C16 C1
FDA UDI
Class IIActive
Perfit FS FH B40 C4
FDA UDI
Class IIActive
Perfit ZR NU 20 BL3SM W
FDA UDI
Class IActive
Perfit ZR NU 14 BL3 W
FDA UDI
Class IActive
RAYZir FS FH I12 A4M
FDA UDI
Class IIActive
Perfit ZR NA 20 B4 W
FDA UDI
Class IIActive
Perfit ZR NP 14 C3 W
FDA UDI
Class IIActive
Perfit ZR NU 25 A3TM W
FDA UDI
Class IIActive
Perfit FS FH B32 BL3
FDA UDI
Class IIActive
Perfit FS FH C16 D2M
FDA UDI
Class IIActive
Perfit ZR NU 20 C4TM W
FDA UDI
Class IIActive
Perfit ZR NU 16 A3TM W
FDA UDI
Class IIActive
Perfit ZR NU 16 A1TM W
FDA UDI
Class IIActive
Perfit ZR NA 10 C3 W
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Establishments (1)

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

  • Vatech mcis Co., Ltd. Suwon-si Gyeonggi · KR FEI 3019784699