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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 17 of 25
DeviceModel / ReferenceRegistriesClassStatus
St STDAR55
FDA UDI
Class IIActive
Si SIDAR6075H
FDA UDI
Class IIActive
Universal Prosthetic Kit UDH20L
FDA UDI
Class IActive
Si NSIR5011S
FDA UDI
Class IIActive
Si NSIR4008S
FDA UDI
Class IIActive
Surgical Kit DI4L
FDA UDI
Class IActive
S-Guide Kit TDR4070
FDA UDI
Class IActive
Si SBCSN43
FDA UDI
Class IActive
evertis ZTBC45044H
FDA UDI
Class IActive
S-Guide Kit GS57
FDA UDI
Class IActive
S-Guide Kit TDR3511
FDA UDI
Class IActive
Si SFPUR50HS
FDA UDI
Class IActive
Se EBCR5044H
FDA UDI
Class IActive
St STDAW70C
FDA UDI
Class IIActive
St STAGAR20
FDA UDI
Class IIActive
S-Guide Kit FDMH
FDA UDI
Class IActive
Si SBCR6043H
FDA UDI
Class IActive
Si SDAR6071H
FDA UDI
Class IIActive
Si SIN3513S
FDA UDI
Class IIActive
Si NSHAR4533
FDA UDI
Class IIActive
Si SDAR5042H
FDA UDI
Class IIActive
Surgical Kit TWMA00S
FDA UDI
Class IActive
Surgical Kit LLD2308
FDA UDI
Class IActive
ever GUIDE KIT GFDHN
FDA UDI
Class IActive
Si SDAN4571H
FDA UDI
Class IIActive
Si SSPAR4071
FDA UDI
Class IIActive
Si SHAR5570
FDA UDI
Class IIActive
Si SIDAN4056
FDA UDI
Class IIActive
Si SBCN5064H
FDA UDI
Class IActive
S-Guide Kit TDW3511
FDA UDI
Class IActive
Surgical Kit HFD00RS
FDA UDI
Class IActive
Si SIDAN4054H
FDA UDI
Class IIActive
Si SFTR40HL
FDA UDI
Class IActive
Si SICAN4030
FDA UDI
Class IIActive
Si STAR4530HP
FDA UDI
Class IActive
evertis TBBCSR64
FDA UDI
Class IActive
evertis NSSD4008
FDA UDI
Class IActive
St STBCSR42
FDA UDI
Class IActive
evertis TBBCR5044R
FDA UDI
Class IActive
Se EBCR5042H
FDA UDI
Class IActive
Surgical Kit DP00S
FDA UDI
Class IActive
evertis TTBCSN31
FDA UDI
Class IActive
Sinus Kit SIST08
FDA UDI
Class IActive
Si SIR5007SF
FDA UDI
Class IIActive
Si SFTR40L
FDA UDI
Class IActive
Si SAA4525R20
FDA UDI
Class IIActive
St STCTAR20C
FDA UDI
Class IIActive
Si NSHAR6022
FDA UDI
Class IIActive
Si SIDAN4555
FDA UDI
Class IIActive
Si SBCR6044H
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