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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 19 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SSA45R40
FDA UDI
Class IIActive
St STCSR
FDA UDI
Class IIActive
evertis TTBCW6641C
FDA UDI
Class IActive
Si SFTR40HS
FDA UDI
Class IActive
Si SBCSN66
FDA UDI
Class IActive
Si SSPAN4052
FDA UDI
Class IIActive
Sm MB3010SR
FDA UDI
Class IIActive
Si NSIN3513SF
FDA UDI
Class IIActive
Si NSHAR4546
FDA UDI
Class IIActive
Si SFTR50HL
FDA UDI
Class IActive
Si SDAR5073H
FDA UDI
Class IIActive
Si NSHAR6035
FDA UDI
Class IIActive
Si SSPAN4554
FDA UDI
Class IIActive
Sm MB3010LR
FDA UDI
Class IIActive
S-Guide Kit TDW3570
FDA UDI
Class IActive
St STR4511LS
FDA UDI
Class IIActive
Si STAN4010HP
FDA UDI
Class IActive
Si SSA45R10
FDA UDI
Class IIActive
evertis ZTBC56065H
FDA UDI
Class IActive
Si SSPBC50S
FDA UDI
Class IActive
St STBCR5031C
FDA UDI
Class IActive
St STW5013SS
FDA UDI
Class IIActive
ever GUIDE KIT GFD5013
FDA UDI
Class IActive
S-Guide Kit TP45
FDA UDI
Class IActive
Si SHAR4070
FDA UDI
Class IIActive
Si SSPAC40
FDA UDI
Class IActive
Surgical Kit LSD3511
FDA UDI
Class IActive
Si SDAN5075H
FDA UDI
Class IIActive
evertis TBBCSS66
FDA UDI
Class IActive
Si SIDAR6044
FDA UDI
Class IIActive
Si NSHAN4023
FDA UDI
Class IIActive
Si NSIR4513SF
FDA UDI
Class IIActive
Si SFTR40S
FDA UDI
Class IActive
Si SSPAR6052
FDA UDI
Class IIActive
Si SIDAR5044
FDA UDI
Class IIActive
Si SFPUR60HS
FDA UDI
Class IActive
Si SDAN5071H
FDA UDI
Class IIActive
ever GUIDE KIT GFD4008
FDA UDI
Class IActive
evertis TTBCR5031C
FDA UDI
Class IActive
Si SIDAR5042H
FDA UDI
Class IIActive
Si SSPAR4054
FDA UDI
Class IIActive
Sinus Kit SHSC1
FDA UDI
Class IActive
Surgical Kit LCB45
FDA UDI
Class IActive
Si SDAN5073H
FDA UDI
Class IIActive
ever GUIDE KIT GMDTW
FDA UDI
Class IActive
Si SAT55
FDA UDI
Class IActive
Si SBCN5044H
FDA UDI
Class IActive
Surgical Kit DG00
FDA UDI
Class IActive
Si SDAR6055H
FDA UDI
Class IIActive
Si SSPAN4041
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