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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 13 of 25
DeviceModel / ReferenceRegistriesClassStatus
evertis TTBCN5062R
FDA UDI
Class IActive
Si SIDAR6041
FDA UDI
Class IIActive
Si SHAR5035
FDA UDI
Class IIActive
Repair Kit RKARR
FDA UDI
Class IActive
Surgical Kit TWFA00REL
FDA UDI
Class IActive
evertis ZTBC45064H
FDA UDI
Class IActive
Si SSPAR6041
FDA UDI
Class IIActive
Si SIDAR6075
FDA UDI
Class IIActive
Si STAR5020
FDA UDI
Class IIActive
Si STAR5030P
FDA UDI
Class IActive
St STR4007LSF
FDA UDI
Class IIActive
Si SDAN5042
FDA UDI
Class IIActive
Surgical Kit LSD5015
FDA UDI
Class IActive
Si STAR4510H
FDA UDI
Class IIActive
Repair Kit RKMIG
FDA UDI
Class IActive
St STR4507LSF
FDA UDI
Class IIActive
S-Guide Kit TDR4510
FDA UDI
Class IActive
Si SIDAR6073
FDA UDI
Class IIActive
S-Guide Kit SD85
FDA UDI
Class IActive
Si SSPICC4055
FDA UDI
Class IActive
ever GUIDE KIT GFD4508
FDA UDI
Class IActive
Se EBCW5066H
FDA UDI
Class IActive
evertis NSSD5008
FDA UDI
Class IActive
Surgical Kit TWFA02NS
FDA UDI
Class IActive
Si SSPAA4040
FDA UDI
Class IActive
Si SSPAA4570
FDA UDI
Class IActive
Si SSA55R40
FDA UDI
Class IIActive
evertis ZTBCS42
FDA UDI
Class IActive
Si NSHAR5533
FDA UDI
Class IIActive
ever GUIDE KIT GCB50
FDA UDI
Class IActive
evertis TBBCS4066R
FDA UDI
Class IActive
Si SICAR5530
FDA UDI
Class IIActive
St STCTAW40
FDA UDI
Class IIActive
Si SBA45R10
FDA UDI
Class IIActive
Si SFPUN40S
FDA UDI
Class IActive
Si SIDAR5055
FDA UDI
Class IIActive
Si SIR5015S
FDA UDI
Class IIActive
St STHAW20
FDA UDI
Class IIActive
Sinus Kit SKRP37
FDA UDI
Class IActive
Si SAS18
FDA UDI
Class IIActive
Si SSPAA6070
FDA UDI
Class IActive
Si SIDAN4552
FDA UDI
Class IIActive
Si SDAR4544H
FDA UDI
Class IIActive
S-Guide Kit ID226
FDA UDI
Class IActive
St STR3515SSF
FDA UDI
Class IIActive
Sm MB3008LR
FDA UDI
Class IIActive
St STMAR00
FDA UDI
Class IIActive
ever GUIDE KIT GPD5006
FDA UDI
Class IActive
Si NSIR4508S
FDA UDI
Class IIActive
S-Guide Kit ASL
FDA UDI
Class IActive

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