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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 4 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SIR5507SF
FDA UDI
Class IIActive
Si SDAR5075H
FDA UDI
Class IIActive
Si SICAN4015
FDA UDI
Class IIActive
Si SIDAN4055H
FDA UDI
Class IIActive
Surgical Kit SBPR52
FDA UDI
Class IActive
St STBCSW62
FDA UDI
Class IActive
S-Guide Kit AD10
FDA UDI
Class IActive
S-Guide Kit TDW4510
FDA UDI
Class IActive
Si SAA4515N20
FDA UDI
Class IIActive
Si SAA5525R20HF
FDA UDI
Class IIActive
Si SBCR6064H
FDA UDI
Class IActive
Universal Prosthetic Kit UDS00S
FDA UDI
Class IActive
Si SSPAR6044
FDA UDI
Class IIActive
Si SIN3508SF
FDA UDI
Class IIActive
St STCTAW20C
FDA UDI
Class IIActive
Si NSIR7008S
FDA UDI
Class IIActive
Si SFPUR40L
FDA UDI
Class IActive
Si SSPAR5041
FDA UDI
Class IIActive
Si SIR5510S
FDA UDI
Class IIActive
Si SDAR5055
FDA UDI
Class IIActive
S-Guide Kit TDR4570
FDA UDI
Class IActive
Si SDAR6045
FDA UDI
Class IIActive
Si SSPAR4052
FDA UDI
Class IIActive
Si SIDAR5054H
FDA UDI
Class IIActive
Surgical Kit SSD2011A
FDA UDI
Class IActive
Si SBCR5042H
FDA UDI
Class IActive
Surgical Kit LSD4513
FDA UDI
Class IActive
Si SIR4010SF
FDA UDI
Class IIActive
Surgical Kit LSSSK01
FDA UDI
Class IActive
Si SSPAR4553
FDA UDI
Class IIActive
Si SIN3508S
FDA UDI
Class IIActive
Si SSPAN4572
FDA UDI
Class IIActive
Si SBA35R20
FDA UDI
Class IIActive
Short Drill Kit SDK
FDA UDI
Class IActive
Si SIDAR5075
FDA UDI
Class IIActive
Si SFTR60HS
FDA UDI
Class IActive
Se EBCSN66
FDA UDI
Class IActive
St STCTAW20
FDA UDI
Class IIActive
Si SMAN01
FDA UDI
Class IIActive
Si SSPBC50B
FDA UDI
Class IActive
Si SSPAA4070
FDA UDI
Class IActive
Si STAN4010
FDA UDI
Class IIActive
S-Guide Kit FMR
FDA UDI
Class IActive
St STR4508LS
FDA UDI
Class IIActive
St STW4508SSF
FDA UDI
Class IIActive
Si SDAR4555H
FDA UDI
Class IIActive
evertis TBBCS4064R
FDA UDI
Class IActive
Si SIDAN5052H
FDA UDI
Class IIActive
evertis ZTBC35066H
FDA UDI
Class IActive
Sm MB2511SR
FDA UDI
Class IIActive

Related Companies

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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