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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 6 of 25
DeviceModel / ReferenceRegistriesClassStatus
ever GUIDE KIT GCB40
FDA UDI
Class IActive
ever GUIDE KIT GFD4013
FDA UDI
Class IActive
Si SFTN40S
FDA UDI
Class IActive
Si SDAR5075
FDA UDI
Class IIActive
Trial Kit - Luna S F40 STRK40
FDA UDI
Class IActive
ever GUIDE KIT GCB45
FDA UDI
Class IActive
Si SSPAR5072
FDA UDI
Class IIActive
St STR4007SS
FDA UDI
Class IIActive
ever GUIDE KIT GFDTWR
FDA UDI
Class IActive
Surgical Kit TWBAA01
FDA UDI
Class IActive
Si SIDAR5041
FDA UDI
Class IIActive
ever GUIDE KIT GPD5004
FDA UDI
Class IActive
Surgical Kit EDS00S
FDA UDI
Class IActive
Si SDAR6072
FDA UDI
Class IIActive
evertis TBBCR5064R
FDA UDI
Class IActive
Se EBCSN44
FDA UDI
Class IActive
Surgical Kit SHS01L
FDA UDI
Class IActive
evertis NSSD4511
FDA UDI
Class IActive
Si NSIN3511SF
FDA UDI
Class IIActive
Si SSPAR5044
FDA UDI
Class IIActive
Surgical Kit GG00
FDA UDI
Class IActive
Si SIDAR5045H
FDA UDI
Class IIActive
St STR4008SSF
FDA UDI
Class IIActive
Surgical Kit SHHS00ES
FDA UDI
Class IActive
Si STC55SP
FDA UDI
Class IActive
St STSPAW70
FDA UDI
Class IIActive
Surgical Kit LCB50
FDA UDI
Class IActive
Si SSPAR5045
FDA UDI
Class IIActive
S-Guide Kit TDW4511
FDA UDI
Class IActive
Si SIDAR5057H
FDA UDI
Class IIActive
Si SDAR4572H
FDA UDI
Class IIActive
evertis TTBCR5041C
FDA UDI
Class IActive
Surgical Kit LSD4508
FDA UDI
Class IActive
Surgical Kit DI4S
FDA UDI
Class IActive
Surgical Kit LSD3510
FDA UDI
Class IActive
Si SIR4507S
FDA UDI
Class IIActive
Si SIR6013S
FDA UDI
Class IIActive
St STMAW00
FDA UDI
Class IIActive
Si SBCR5043H
FDA UDI
Class IActive
Si SPP55H
FDA UDI
Class IActive
Si SSPAA4055
FDA UDI
Class IActive
Si SIDAN4052H
FDA UDI
Class IIActive
ever GUIDE KIT GTP35
FDA UDI
Class IActive
Si SBCN5066H
FDA UDI
Class IActive
St STHAR30
FDA UDI
Class IIActive
Si SAPU45
FDA UDI
Class IActive
Surgical Kit LLD2315
FDA UDI
Class IActive
Si SDAR6042H
FDA UDI
Class IIActive
evertis TTBCN5042R
FDA UDI
Class IActive
Si SHAN5070
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

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