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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 15 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SDAN4553
FDA UDI
Class IIActive
evertis SSD2210
FDA UDI
Class IActive
Si SIDAR5053
FDA UDI
Class IIActive
evertis ZTBCS66
FDA UDI
Class IActive
Surgical Kit LSD4510
FDA UDI
Class IActive
Si SHAR6020
FDA UDI
Class IIActive
Si SAA5525R40
FDA UDI
Class IIActive
St STCTAR40C
FDA UDI
Class IIActive
evertis TBBCSS42
FDA UDI
Class IActive
Si SSPAR4574
FDA UDI
Class IIActive
Si SFPUN40HL
FDA UDI
Class IActive
Si SIDAR4555
FDA UDI
Class IIActive
Se EBCW5064H
FDA UDI
Class IActive
Si SBCN5042H
FDA UDI
Class IActive
Surgical Kit TW00
FDA UDI
Class IActive
Si NSIR6008S
FDA UDI
Class IIActive
Si SSPAR6074
FDA UDI
Class IIActive
Si NSHAR4035
FDA UDI
Class IIActive
St STBCW6031C
FDA UDI
Class IActive
Si SIDAN4053
FDA UDI
Class IIActive
Surgical Kit LSD5011
FDA UDI
Class IActive
Surgical Kit TWHA00L
FDA UDI
Class IActive
Si SHAR6520
FDA UDI
Class IIActive
Si SAA4525R20H
FDA UDI
Class IIActive
evertis TTBCSN62
FDA UDI
Class IActive
Sinus Kit SITD7503
FDA UDI
Class IActive
St STAGAR15
FDA UDI
Class IIActive
Si SIDAN4557
FDA UDI
Class IIActive
Surgical Kit TWFA02RL
FDA UDI
Class IActive
Sinus Kit SIST09
FDA UDI
Class IActive
Si SIDAR4552H
FDA UDI
Class IIActive
S-Guide Kit ASS
FDA UDI
Class IActive
Repair Kit RKGH00
FDA UDI
Class IActive
Si STC40S
FDA UDI
Class IIActive
Surgical Kit LSD4007
FDA UDI
Class IActive
Surgical Kit SSD5013A
EUDAMEDFDA UDI
Class IActive
Si SBCR5064H
FDA UDI
Class IActive
Si SICAR4015
FDA UDI
Class IIActive
Si NSHAR6034
FDA UDI
Class IIActive
S-Guide Kit TDR4511
FDA UDI
Class IActive
St STW4511LSF
FDA UDI
Class IIActive
evertis TBBCS4044R
FDA UDI
Class IActive
St STR3511SS
FDA UDI
Class IIActive
Si SBCR6065H
FDA UDI
Class IActive
Si SIDAR5043H
FDA UDI
Class IIActive
Si SHAR4535
FDA UDI
Class IIActive
Surgical Kit SSD4015A
EUDAMEDFDA UDI
Class IActive
Si SICAN4030H
FDA UDI
Class IIActive
S-Guide Kit NMDW
FDA UDI
Class IActive
Surgical Kit SHHS00S
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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