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Shinhung MST Co., Ltd.

US

Last updated May 24, 2026

What Shinhung MST Co., Ltd. makes

Shinhung MST Co., Ltd. manufactures dental implant suprastructures, including permanent and temporary preformed designs, as well as kits for dental implant procedures. Their portfolio also includes screw endosteal dental implants in both one-piece and two-piece configurations, reusable dental drill bits, and various surgical procedure kits for dental and maxillofacial applications. These products are designed for single-use and reusable medical settings, depending on the device type.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are regulated under U.S. medical device laws, ensuring compliance with applicable standards for dental and surgical instruments. The manufacturer operates from 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 Shinhung MST Co., Ltd. primarily manufacture?

Shinhung MST Co., Ltd. specializes in dental and maxillofacial medical devices. Their portfolio includes dental implant suprastructures (both permanent and temporary preformed types), screw endosteal dental implants (available in one-piece or two-piece designs), reusable dental drill bits, and various surgical procedure kits. These kits are designed for dental and maxillofacial procedures, with some intended for single-use and others for reusable applications.

Where is Shinhung MST Co., Ltd. based, and how does this affect their regulatory compliance?

Shinhung MST Co., Ltd. is based in the United States, which means their devices are subject to U.S. medical device regulations. Since they operate within the U.S., their products must comply with FDA requirements, including classification under FDA’s regulatory framework (Class I or Class II) and registration in the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries or databases list Shinhung MST Co., Ltd.’s devices?

Shinhung MST Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are Shinhung MST Co., Ltd.’s devices classified under U.S. regulations?

Shinhung MST Co., Ltd.’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and regulatory history.

What kinds of surgical kits does Shinhung MST Co., Ltd. produce, and how are they categorized?

Shinhung MST Co., Ltd. manufactures both dental implant procedure kits and general/maxillofacial surgical kits. These kits are categorized based on their intended use—some are designed for single-use (non-medicated), while others are reusable. For example, their dental/maxillofacial surgical kits are reusable, whereas general surgical procedure kits may be intended for single-use applications, depending on the specific product.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+821099545139
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
689667152

Catalogue (1225)

Page 22 of 25
DeviceModel / ReferenceRegistriesClassStatus
St STHAW30
FDA UDI
Class IIActive
Si NSHAR5046
FDA UDI
Class IIActive
Si SDAR4541H
FDA UDI
Class IIActive
Si SSPAR6053
FDA UDI
Class IIActive
Si SDAR4553
FDA UDI
Class IIActive
S-Guide Kit FDRH
FDA UDI
Class IActive
St STCSWL
FDA UDI
Class IIActive
Surgical Kit SSD4008A
EUDAMEDFDA UDI
Class IActive
Si SDAR6075
FDA UDI
Class IIActive
Si SSPAN4043
FDA UDI
Class IIActive
Si SIDAR5043
FDA UDI
Class IIActive
Si SDAR4552H
FDA UDI
Class IIActive
Sinus Kit SIST05
FDA UDI
Class IActive
Si SSPAC45
FDA UDI
Class IActive
Si NSHAR4522
FDA UDI
Class IIActive
Si SAA55
FDA UDI
Class IActive
Si SIDAR6055H
FDA UDI
Class IIActive
Si SDAR6052
FDA UDI
Class IIActive
Si SDAR4543
FDA UDI
Class IIActive
St STW4507LS
FDA UDI
Class IIActive
Si SDAR6053
FDA UDI
Class IIActive
Si SDAR6051
FDA UDI
Class IIActive
ever GUIDE KIT GID2605
FDA UDI
Class IActive
evertis TBBCSR65
FDA UDI
Class IActive
St STDAR55C
FDA UDI
Class IIActive
Si SIDAR6055
FDA UDI
Class IIActive
Se EBCN5064H
FDA UDI
Class IActive
Si NSHAN4046
FDA UDI
Class IIActive
Surgical Kit H09D02S
FDA UDI
Class IActive
St STBCSR62
FDA UDI
Class IActive
evertis SSG53C
FDA UDI
Class IActive
Repair Kit RKSRDR
FDA UDI
Class IActive
Si SFTSR00S
FDA UDI
Class IActive
Surgical Kit SLMD200S
FDA UDI
Class IActive
Surgical Kit LSD4515
FDA UDI
Class IActive
Si SFTR50HS
FDA UDI
Class IActive
Si SSPAN4543
FDA UDI
Class IIActive
St STR4013SSF
FDA UDI
Class IIActive
Si SDAR4571
FDA UDI
Class IIActive
S-Guide Kit SD70
FDA UDI
Class IActive
St STBCSW31
FDA UDI
Class IActive
Si NSIR5013S
FDA UDI
Class IIActive
Se EBCW5042H
FDA UDI
Class IActive
Si NSHAN4035
FDA UDI
Class IIActive
Surgical Kit SMA02S
FDA UDI
Class IActive
evertis ZTBCS45
FDA UDI
Class IActive
Si SFAR40
FDA UDI
Class IActive
evertis ZTBC56066H
FDA UDI
Class IActive
evertis TBBCSR66
FDA UDI
Class IActive
Si BAS00A
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

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

  • Shinhung MST Co., Ltd. Wonju Si Gangwon · KR FEI 3006948193