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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 7 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SSPAC50
FDA UDI
Class IActive
St STAGAR15C
FDA UDI
Class IIActive
Sinus Kit SIST04
FDA UDI
Class IActive
Sinus Kit SIST03
FDA UDI
Class IActive
ever GUIDE KIT GLD2608
FDA UDI
Class IActive
Surgical Kit HFD01NEL
FDA UDI
Class IActive
Surgical Kit TWFA02NL
FDA UDI
Class IActive
Si SPUSN00L
FDA UDI
Class IActive
Si SPUSR00L
FDA UDI
Class IActive
Surgical Kit TWFA00RS
FDA UDI
Class IActive
Si SSPAA4555
FDA UDI
Class IActive
St STR3508LS
FDA UDI
Class IIActive
Si SSPAR4541
FDA UDI
Class IIActive
evertis NSSD4510
FDA UDI
Class IActive
Si SDAN4552H
FDA UDI
Class IIActive
Si SFPUN40L
FDA UDI
Class IActive
Surgical Kit SSD2013A
FDA UDI
Class IActive
Si SIDAR6052H
FDA UDI
Class IIActive
St STR4507LS
FDA UDI
Class IIActive
ever GUIDE KIT GFD5011
FDA UDI
Class IActive
Si SSPBC45B
FDA UDI
Class IActive
Si SBA35R50
FDA UDI
Class IIActive
St STR3508SSF
FDA UDI
Class IIActive
Si SFPUR60S
FDA UDI
Class IActive
St STW5011SSF
FDA UDI
Class IIActive
Si SSPAR5051
FDA UDI
Class IIActive
evertis NSSD4507
FDA UDI
Class IActive
ever GUIDE KIT GFD3508
FDA UDI
Class IActive
Si SIDAR6071H
FDA UDI
Class IIActive
Si SDAR5044H
FDA UDI
Class IIActive
Surgical Kit LITD60D
FDA UDI
Class IActive
S-Guide Kit TDW5013
FDA UDI
Class IActive
St STDAW40
FDA UDI
Class IIActive
Surgical Kit SBPR55A
FDA UDI
Class IActive
Sinus Kit SIST10
FDA UDI
Class IActive
Si STAR5030
FDA UDI
Class IIActive
Surgical Kit TWMA02L
FDA UDI
Class IActive
Surgical Kit STTWFA01S
FDA UDI
Class IActive
evertis ZTBC35044H
FDA UDI
Class IActive
Surgical Kit LSD4015
FDA UDI
Class IActive
Si SFTN40HL
FDA UDI
Class IActive
Si SSPAR5052
FDA UDI
Class IIActive
Si SAA5515R40H
FDA UDI
Class IIActive
Si NSHAR4033
FDA UDI
Class IIActive
Surgical Kit TWFA00NEL
FDA UDI
Class IActive
Si SDAN5071
FDA UDI
Class IIActive
evertis TBBCN5044R
FDA UDI
Class IActive
Surgical Kit SSD4010A
EUDAMEDFDA UDI
Class IActive
Universal Prosthetic Kit UDH25L
FDA UDI
Class IActive
Si SBA35N50
FDA UDI
Class IIActive

Related Companies

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Importers

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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