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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 9 of 25
DeviceModel / ReferenceRegistriesClassStatus
Surgical Kit SSD5010A
EUDAMEDFDA UDI
Class IActive
Si SSPICC4555
FDA UDI
Class IActive
Si SIR7008S
FDA UDI
Class IIActive
Si SIDAR5075H
FDA UDI
Class IIActive
Si SIDAR6054
FDA UDI
Class IIActive
Si NSIR6010SF
FDA UDI
Class IIActive
evertis NCB50
FDA UDI
Class IActive
Si SIDAR4553H
FDA UDI
Class IIActive
Si SIR5010S
FDA UDI
Class IIActive
Surgical Kit LSK02
FDA UDI
Class IActive
Si SIDAR6053H
FDA UDI
Class IIActive
S-Guide Kit TDR3585
FDA UDI
Class IActive
Si SSPAN4073
FDA UDI
Class IIActive
Guide Kit EGKC
FDA UDI
Class IActive
Si NSIR4007SF
FDA UDI
Class IIActive
Repair Kit RKSRT
FDA UDI
Class IActive
Si SIDAR4557
FDA UDI
Class IIActive
Si SDAR5043
FDA UDI
Class IIActive
Si SIDAR4551H
FDA UDI
Class IIActive
Si SSPAR4573
FDA UDI
Class IIActive
Si SSPAR6073
FDA UDI
Class IIActive
Si STC45SP
FDA UDI
Class IActive
Si SDAR6052H
FDA UDI
Class IIActive
Surgical Kit SSD4013A
EUDAMEDFDA UDI
Class IActive
Si SHAR5520
FDA UDI
Class IIActive
evertis TTBCN5041R
FDA UDI
Class IActive
S-Guide Kit TDR3570
FDA UDI
Class IActive
Si SIDAN4056H
FDA UDI
Class IIActive
Si SIDAN4057
FDA UDI
Class IIActive
Si SIDAR6072H
FDA UDI
Class IIActive
evertis SSD2215
FDA UDI
Class IActive
ever GUIDE KIT GFD4510
FDA UDI
Class IActive
Sm MB2508LR
FDA UDI
Class IIActive
Si NSHAN4534
FDA UDI
Class IIActive
ever GUIDE KIT GFD4511
FDA UDI
Class IActive
Si SIR4013SF
FDA UDI
Class IIActive
St STCTAW40C
FDA UDI
Class IIActive
Surgical Kit TWMA01L
FDA UDI
Class IActive
Si SSPAN4044
FDA UDI
Class IIActive
Si NSHAR4034
FDA UDI
Class IIActive
Si BAA45
FDA UDI
Class IActive
Repair Kit RKSTG
FDA UDI
Class IActive
S-Guide Kit TDR4011
FDA UDI
Class IActive
evertis ZTBCS44
FDA UDI
Class IActive
S-Guide Kit TP50W
FDA UDI
Class IActive
Si SSPAR5043
FDA UDI
Class IIActive
Si SSPAR6042
FDA UDI
Class IIActive
evertis NSSD4013
FDA UDI
Class IActive
Si SDAR5051
FDA UDI
Class IIActive
Si SDAR6073H
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

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