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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 5 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SSPAN4573
FDA UDI
Class IIActive
Sinus Kit SHSC2
FDA UDI
Class IActive
Si SBA45R20
FDA UDI
Class IIActive
Si SIR4011SF
FDA UDI
Class IIActive
ever GUIDE KIT GFD5008
FDA UDI
Class IActive
Si NSIR7010S
FDA UDI
Class IIActive
Surgical Kit SMA01S
FDA UDI
Class IActive
S-Guide Kit TDR4013
FDA UDI
Class IActive
St STDAW55
FDA UDI
Class IIActive
Si SICAR5515H
FDA UDI
Class IIActive
Repair Kit RKLNGN
FDA UDI
Class IActive
Si SDAR6055
FDA UDI
Class IIActive
St STR4007LS
FDA UDI
Class IIActive
Sinus Kit SIDR42
FDA UDI
Class IActive
St STR4513SS
FDA UDI
Class IIActive
Si SIR5007S
FDA UDI
Class IIActive
evertis TTBCW6642C
FDA UDI
Class IActive
ever GUIDE KIT GFD5005
FDA UDI
Class IActive
Si SSPAR4042
FDA UDI
Class IIActive
Si SASR
FDA UDI
Class IIActive
evertis TTBCSN42
FDA UDI
Class IActive
Sinus Kit SIDR32
FDA UDI
Class IActive
Surgical Kit STTWFA02S
FDA UDI
Class IActive
Si SAPU40
FDA UDI
Class IActive
Si SAA4525N40HF
FDA UDI
Class IIActive
Si SAPU40H
FDA UDI
Class IActive
Si SFPUR50L
FDA UDI
Class IActive
Si SIR6007S
FDA UDI
Class IIActive
Surgical Kit LLD2307
FDA UDI
Class IActive
Si SAT40H
FDA UDI
Class IActive
Si SAT45H
FDA UDI
Class IActive
Si SIDAR5073
FDA UDI
Class IIActive
Sinus Kit SKBC00
FDA UDI
Class IActive
Si SSPAR6071
FDA UDI
Class IIActive
Si STAN4030H
FDA UDI
Class IIActive
ever GUIDE KIT GFD5007
FDA UDI
Class IActive
Si SFPUN40HS
FDA UDI
Class IActive
Si SIDAR4553
FDA UDI
Class IIActive
evertis NSSD5013
FDA UDI
Class IActive
Surgical Kit SBPR55
FDA UDI
Class IActive
evertis ZTBC56044H
FDA UDI
Class IActive
Se EBCN5044H
FDA UDI
Class IActive
Universal Prosthetic Kit UDS00L
FDA UDI
Class IActive
Si SAPU55H
FDA UDI
Class IActive
Si SSA55R20
FDA UDI
Class IIActive
Si SDAR5072
FDA UDI
Class IIActive
S-Guide Kit FMW
FDA UDI
Class IActive
evertis NSSD4513
FDA UDI
Class IActive
Se EBCSR44
FDA UDI
Class IActive
S-Guide Kit SD10
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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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