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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 20 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SHAN4570
FDA UDI
Class IIActive
Si SIDAR5071
FDA UDI
Class IIActive
Si SIDAR6073H
FDA UDI
Class IIActive
Si SBA35R40
FDA UDI
Class IIActive
Se EBCSW44
FDA UDI
Class IActive
evertis NSSD5010
FDA UDI
Class IActive
S-Guide Kit TDW4513
FDA UDI
Class IActive
ever GUIDE KIT GFD5006
FDA UDI
Class IActive
Surgical Kit SHHS00L
FDA UDI
Class IActive
Sm MB3013LR
FDA UDI
Class IIActive
Si STAR5020H
FDA UDI
Class IIActive
St STW4510LS
FDA UDI
Class IIActive
St STR3508LSF
FDA UDI
Class IIActive
Si SIDAR5052
FDA UDI
Class IIActive
evertis SSD2208
FDA UDI
Class IActive
Si SDAN5072
FDA UDI
Class IIActive
Si NSHAR6033
FDA UDI
Class IIActive
Surgical Kit SSD3508A
FDA UDI
Class IActive
Surgical Kit DI5S
FDA UDI
Class IActive
S-Guide Kit CDW
FDA UDI
Class IActive
Si SDAR4554
FDA UDI
Class IIActive
Surgical Kit LSD5007
FDA UDI
Class IActive
St STAGAR20C
FDA UDI
Class IIActive
Surgical Kit SSD5015A
FDA UDI
Class IActive
ever GUIDE KIT GID2604
FDA UDI
Class IActive
Sinus Kit SIST06
FDA UDI
Class IActive
ever GUIDE KIT GFD4007
FDA UDI
Class IActive
Surgical Kit SPD200L
FDA UDI
Class IActive
Si STC40B
FDA UDI
Class IIActive
Si SIR5513SF
FDA UDI
Class IIActive
ever GUIDE KIT RW00
FDA UDI
Class IActive
Surgical Kit SMA01L
FDA UDI
Class IActive
Si SFTSR00L
FDA UDI
Class IActive
Sinus Kit SIDR2804
FDA UDI
Class IActive
Si SSPAN4042
FDA UDI
Class IIActive
evertis SSG53P
FDA UDI
Class IActive
St STDAW55C
FDA UDI
Class IIActive
Si SIDAR5055H
FDA UDI
Class IIActive
Si SDAR6044
FDA UDI
Class IIActive
Si SSPAR4074
FDA UDI
Class IIActive
Se EBCSR66
FDA UDI
Class IActive
Universal Prosthetic Kit UDH25S
FDA UDI
Class IActive
ever GUIDE KIT GFDTWN
FDA UDI
Class IActive
Si SBA45R50
FDA UDI
Class IIActive
St STDAR70
FDA UDI
Class IIActive
Surgical Kit STDK
FDA UDI
Class IActive
Si SDAN4572
FDA UDI
Class IIActive
Si SBCSR42
FDA UDI
Class IActive
S-Guide Kit TP35
FDA UDI
Class IActive
Si SIDAR5071H
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