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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 3 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SHAN4550
FDA UDI
Class IIActive
Si SPP45H
FDA UDI
Class IActive
Si SICAR4015H
FDA UDI
Class IIActive
Si STAN4010H
FDA UDI
Class IIActive
Si SIDAN4552H
FDA UDI
Class IIActive
Si SATS18
FDA UDI
Class IActive
evertis TTBCW6662C
FDA UDI
Class IActive
Surgical Kit TWMA00L
FDA UDI
Class IActive
ever GUIDE KIT GPD5005
FDA UDI
Class IActive
ever GUIDE KIT GFD3513
FDA UDI
Class IActive
St STHAR40
FDA UDI
Class IIActive
Si SDAR4551
FDA UDI
Class IIActive
Si SSPAR6075
FDA UDI
Class IIActive
Si SBA35N20
FDA UDI
Class IIActive
Si SASN
FDA UDI
Class IIActive
Si SSPAR5074
FDA UDI
Class IIActive
St STR3515SS
FDA UDI
Class IIActive
Sm MB2510SR
FDA UDI
Class IIActive
Si SIDAR6042H
FDA UDI
Class IIActive
Si SBA35N60
FDA UDI
Class IIActive
evertis NSSD4011
FDA UDI
Class IActive
Si SSPAR4554
FDA UDI
Class IIActive
Si SFPUR40HS
FDA UDI
Class IActive
St STAGAW20C
FDA UDI
Class IIActive
S-Guide Kit TDR4085
FDA UDI
Class IActive
Si NSHAR5523
FDA UDI
Class IIActive
St STDAR40
FDA UDI
Class IIActive
ever GUIDE KIT GFD4011
FDA UDI
Class IActive
evertis ZTBC45066H
FDA UDI
Class IActive
Si SIR6010SF
FDA UDI
Class IIActive
Si SBA35N30
FDA UDI
Class IIActive
Surgical Kit SSD3507A
FDA UDI
Class IActive
Se EBCW5044H
FDA UDI
Class IActive
S-Guide Kit HGS50
FDA UDI
Class IActive
Si SDAN4574
FDA UDI
Class IIActive
Si SIR7007S
FDA UDI
Class IIActive
Surgical Kit TWSLA00
FDA UDI
Class IActive
S-Guide Kit TDW4570
FDA UDI
Class IActive
Si SCSN00
FDA UDI
Class IIActive
evertis TBBCSS64
FDA UDI
Class IActive
evertis ZTBC45065H
FDA UDI
Class IActive
Repair Kit RKARN
FDA UDI
Class IActive
Si SIDAR6053
FDA UDI
Class IIActive
Si SHAN4020
FDA UDI
Class IIActive
evertis TBBCR5043R
FDA UDI
Class IActive
S-Guide Kit SD13
FDA UDI
Class IActive
Si SDAN4575
FDA UDI
Class IIActive
Si NSIN3510SF
FDA UDI
Class IIActive
Si STAR5020HP
FDA UDI
Class IActive
Surgical Kit TWFA01NL
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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