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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 10 of 25
DeviceModel / ReferenceRegistriesClassStatus
ever GUIDE KIT GFD4010
FDA UDI
Class IActive
Si SFPUR50HL
FDA UDI
Class IActive
Si SSPAN4544
FDA UDI
Class IIActive
Si SIDAR6071
FDA UDI
Class IIActive
Si STAN4030
FDA UDI
Class IIActive
Si SIDAN5051H
FDA UDI
Class IIActive
Si SICAR5530H
FDA UDI
Class IIActive
Si SSA45N10
FDA UDI
Class IIActive
Si NSIR4010SF
FDA UDI
Class IIActive
Si SIR4515SF
FDA UDI
Class IIActive
Surgical Kit SCB50A
FDA UDI
Class IActive
Si SDAR4552
FDA UDI
Class IIActive
Si SHAN4520
FDA UDI
Class IIActive
Si SSA45N40
FDA UDI
Class IIActive
Si SIR6011S
FDA UDI
Class IIActive
Repair Kit RKSRDN
FDA UDI
Class IActive
Taper Kit EVERKC
FDA UDI
Class IActive
Surgical Kit LITD40D
FDA UDI
Class IActive
ever GUIDE KIT GSIDS
FDA UDI
Class IActive
Surgical Kit DI5L
FDA UDI
Class IActive
S-Guide Kit TDW5070
FDA UDI
Class IActive
Surgical Kit STHFD01EL
FDA UDI
Class IActive
Si SIDAR5045
FDA UDI
Class IIActive
Surgical Kit HFD01NL
FDA UDI
Class IActive
Si SDAR5053
FDA UDI
Class IIActive
Si SHAN3550
FDA UDI
Class IIActive
Universal Prosthetic Kit UDU00S
FDA UDI
Class IActive
Si SSPAN4574
FDA UDI
Class IIActive
St STCSW
FDA UDI
Class IIActive
Si SIDAR4555H
FDA UDI
Class IIActive
Surgical Kit TWFA00RL
FDA UDI
Class IActive
Si SIDAN4553H
FDA UDI
Class IIActive
Si SSPAR4571
FDA UDI
Class IIActive
Si SSPAR6054
FDA UDI
Class IIActive
evertis TTBCSN41
FDA UDI
Class IActive
Si SBA35R60
FDA UDI
Class IIActive
Si SIR5511SF
FDA UDI
Class IIActive
Si SSPAR6043
FDA UDI
Class IIActive
Si SIDAR6045H
FDA UDI
Class IIActive
Si SSPBC60S
FDA UDI
Class IActive
Si SBCR5065H
FDA UDI
Class IActive
Surgical Kit SMA0ES
FDA UDI
Class IActive
Si SIDAR6074
FDA UDI
Class IIActive
Si STAR4530
FDA UDI
Class IIActive
Si SAA5525R40HF
FDA UDI
Class IIActive
Si SDAR6054
FDA UDI
Class IIActive
St STTPAW10C
FDA UDI
Class IIActive
St STBCW6041C
FDA UDI
Class IActive
Si STAR4520P
FDA UDI
Class IActive
evertis SSD2213
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