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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 11 of 25
DeviceModel / ReferenceRegistriesClassStatus
Surgical Kit HFD01NS
FDA UDI
Class IActive
Si SSPAR6051
FDA UDI
Class IIActive
Si NSIR4513S
FDA UDI
Class IIActive
Sinus Kit SKDG00
FDA UDI
Class IActive
Si SIDAR4551
FDA UDI
Class IIActive
Si SSPAN4552
FDA UDI
Class IIActive
evertis NSSD3513
FDA UDI
Class IActive
St STR3513LS
FDA UDI
Class IIActive
Si SFTR50L
FDA UDI
Class IActive
Si SIR7013S
FDA UDI
Class IIActive
Si NSHAR6023
FDA UDI
Class IIActive
Si SIDAR6052
FDA UDI
Class IIActive
S-Guide Kit SSGR50C
FDA UDI
Class IActive
Surgical Kit TWFA01NS
FDA UDI
Class IActive
ever GUIDE KIT GFD5010
FDA UDI
Class IActive
Si SBCSR43
FDA UDI
Class IActive
Si SIDAN4053H
FDA UDI
Class IIActive
Surgical Kit SCB45A
FDA UDI
Class IActive
Si SFPUR60L
FDA UDI
Class IActive
Si SDAR5045H
FDA UDI
Class IIActive
S-Guide Kit FDR
FDA UDI
Class IActive
Si SDAN5043H
FDA UDI
Class IIActive
Surgical Kit LITD35D
FDA UDI
Class IActive
Si SAA40
FDA UDI
Class IActive
Si SBCR6066H
FDA UDI
Class IActive
Si SBCSR66
FDA UDI
Class IActive
S-Guide Kit TDW3585
FDA UDI
Class IActive
Si SHAR3520
FDA UDI
Class IIActive
S-Guide Kit TDR3513
FDA UDI
Class IActive
St STR3515LSF
FDA UDI
Class IIActive
Surgical Kit STHFD01S
FDA UDI
Class IActive
evertis ZTBCS43
FDA UDI
Class IActive
Sinus Kit SIST11
FDA UDI
Class IActive
Si SCSR00
FDA UDI
Class IIActive
Si SIDAR5073H
FDA UDI
Class IIActive
Surgical Kit SCB35A
FDA UDI
Class IActive
Si SIDAR5053H
FDA UDI
Class IIActive
Si SIDAR5074H
FDA UDI
Class IIActive
Si STAR4520H
FDA UDI
Class IIActive
Surgical Kit LSD3508
FDA UDI
Class IActive
S-Guide Kit TDW5085
FDA UDI
Class IActive
Surgical Kit SSD2015A
FDA UDI
Class IActive
ever GUIDE KIT GLD2611
FDA UDI
Class IActive
Sinus Kit SKBP00
FDA UDI
Class IActive
St STW4513SS
FDA UDI
Class IIActive
Si STC45B
FDA UDI
Class IIActive
Surgical Kit SBPN50A
FDA UDI
Class IActive
Short Drill Kit DS40
FDA UDI
Class IActive
Surgical Kit TWMA00ES
FDA UDI
Class IActive
Si STC45BP
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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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