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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 2 of 25
DeviceModel / ReferenceRegistriesClassStatus
Repair Kit RKRRD
FDA UDI
Class IActive
Si SDAN4543H
FDA UDI
Class IIActive
Si SSPAN4074
FDA UDI
Class IIActive
Surgical Kit H09D01L
FDA UDI
Class IActive
St STBCSW41
FDA UDI
Class IActive
Si SBA35R10
FDA UDI
Class IIActive
Si SDAN4571
FDA UDI
Class IIActive
S-Guide Kit NMDR
FDA UDI
Class IActive
Si SAA4515R40
FDA UDI
Class IIActive
Si STAR4510HP
FDA UDI
Class IActive
Si SSPAR5054
FDA UDI
Class IIActive
S-Guide Kit CDR
FDA UDI
Class IActive
Surgical Kit LSD4011
FDA UDI
Class IActive
Se EBCSR42
FDA UDI
Class IActive
S-Guide Kit TDW3513
FDA UDI
Class IActive
Si SDAN5051H
FDA UDI
Class IIActive
Si SSPAR5075
FDA UDI
Class IIActive
St STR3510SS
FDA UDI
Class IIActive
evertis ZTBC56064H
FDA UDI
Class IActive
Surgical Kit TWFA01RL
FDA UDI
Class IActive
Surgical Kit LCB40
FDA UDI
Class IActive
Si SSPAA4540
FDA UDI
Class IActive
Si SDAR5043H
FDA UDI
Class IIActive
Sm MB2511LR
FDA UDI
Class IIActive
Si SSPAR4073
FDA UDI
Class IIActive
Si SSPICC6055
FDA UDI
Class IActive
Si SSPAN4542
FDA UDI
Class IIActive
Si SAT45
FDA UDI
Class IActive
Si SHAR3570
FDA UDI
Class IIActive
Si SDAN5053H
FDA UDI
Class IIActive
S-Guide Kit ID356
FDA UDI
Class IActive
Si SSPAN4071
FDA UDI
Class IIActive
Si SIR5513S
FDA UDI
Class IIActive
St STR4013LSF
FDA UDI
Class IIActive
Si SIDAR5042
FDA UDI
Class IIActive
evertis SSD2211
FDA UDI
Class IActive
St STR3510LS
FDA UDI
Class IIActive
Se EBCSW64
FDA UDI
Class IActive
Si SIR4010S
EUDAMEDFDA UDI
Class IIActive
evertis ZTBC45042H
FDA UDI
Class IActive
Si SAA4525N40H
FDA UDI
Class IIActive
Surgical Kit SMA00L
FDA UDI
Class IActive
Si SDAN4542
FDA UDI
Class IIActive
Repair Kit RKLNGR
FDA UDI
Class IActive
Surgical Kit TWFA01NEL
FDA UDI
Class IActive
Si SIDAR5054
FDA UDI
Class IIActive
St STR4010SSF
FDA UDI
Class IIActive
evertis MRTN
FDA UDI
Class IActive
Universal Prosthetic Kit UTWR00
FDA UDI
Class IActive
Si SDAR6072H
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

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