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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 (1226)

Page 1 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SFTSN00L
FDA UDI
Class IActive
St STDAR70C
FDA UDI
Class IIActive
Si SFAN35
FDA UDI
Class IActive
Sm MB3008SR
FDA UDI
Class IIActive
Si SSPAN4051
FDA UDI
Class IIActive
Si SSPAR5071
FDA UDI
Class IIActive
Sinus Kit SIDR2803
FDA UDI
Class IActive
Si SBA35R30
FDA UDI
Class IIActive
S-Guide Kit SSGW50C
FDA UDI
Class IActive
Si SIDAR6042
FDA UDI
Class IIActive
Si SSPAR6045
FDA UDI
Class IIActive
Si SHAN4050
FDA UDI
Class IIActive
ever GUIDE KIT GLD2607
FDA UDI
Class IActive
Surgical Kit H09D00S
FDA UDI
Class IActive
St STAGAW20
FDA UDI
Class IIActive
evertis TBBCN5042R
FDA UDI
Class IActive
ever GUIDE KIT GFD3507
FDA UDI
Class IActive
Surgical Kit TWFA02RS
FDA UDI
Class IActive
Si SICAR4030
FDA UDI
Class IIActive
Si SIR5510SF
FDA UDI
Class IIActive
Si SIDAN4051H
FDA UDI
Class IIActive
Si SSA45N30
FDA UDI
Class IIActive
Si STC55B
FDA UDI
Class IIActive
Si SFPUR40HL
FDA UDI
Class IActive
St STSPAR55
FDA UDI
Class IIActive
Si SSPAR4053
FDA UDI
Class IIActive
Si SIDAR5077H
FDA UDI
Class IIActive
evertis NSSD4010
FDA UDI
Class IActive
Surgical Kit STTWFA01EL
FDA UDI
Class IActive
Si SBCN5043H
FDA UDI
Class IActive
Surgical Kit HFD00NS
FDA UDI
Class IActive
Si SDAN4544H
FDA UDI
Class IIActive
Si SHAN3570
FDA UDI
Class IIActive
evertis ZTBC35064H
FDA UDI
Class IActive
Si SIN3515SF
FDA UDI
Class IIActive
Si SSPAN4054
FDA UDI
Class IIActive
Si SPP40H
FDA UDI
Class IActive
Si SBCR5066H
FDA UDI
Class IActive
evertis NSSD4515
FDA UDI
Class IActive
evertis ZTBC45045H
FDA UDI
Class IActive
Si SSPAN4541
FDA UDI
Class IIActive
Si SSPAN4571
FDA UDI
Class IIActive
Surgical Kit H09D00L
FDA UDI
Class IActive
Se EBCSW66
FDA UDI
Class IActive
Si SIDAN5054H
FDA UDI
Class IIActive
Si SIR4011S
FDA UDI
Class IIActive
Si SIDAR6054H
FDA UDI
Class IIActive
Si SIDAR6041H
FDA UDI
Class IIActive
Surgical Kit LSD4013
FDA UDI
Class IActive
Surgical Kit LSD3507
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

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