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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 14 of 25
DeviceModel / ReferenceRegistriesClassStatus
evertis SSD2207
FDA UDI
Class IActive
ever GUIDE KIT GLD2613
FDA UDI
Class IActive
Si SBA35N10
FDA UDI
Class IIActive
Si SDAR5044
FDA UDI
Class IIActive
Si SAPU45H
FDA UDI
Class IActive
Si SPUSN00S
FDA UDI
Class IActive
Surgical Kit LSD3513
FDA UDI
Class IActive
St STCLSW
FDA UDI
Class IIActive
Surgical Kit SLPK01
FDA UDI
Class IActive
Surgical Kit LSD4507
FDA UDI
Class IActive
evertis TBBCSS43
FDA UDI
Class IActive
Si SBCSR45
FDA UDI
Class IActive
Si SHAN4535
FDA UDI
Class IIActive
S-Guide Kit SGK
FDA UDI
Class IActive
S-Guide Kit TDR3510
FDA UDI
Class IActive
evertis NSSD3515
FDA UDI
Class IActive
Si SIDAN4051
FDA UDI
Class IIActive
Si SSPAR6072
FDA UDI
Class IIActive
Si SIDAR6043
FDA UDI
Class IIActive
Si SIDAN5052
FDA UDI
Class IIActive
S-Guide Kit SD11
FDA UDI
Class IActive
Si SBCSR64
FDA UDI
Class IActive
Si NSIR6011SF
FDA UDI
Class IIActive
Si SDAN5073
FDA UDI
Class IIActive
S-Guide Kit FMM
FDA UDI
Class IActive
Si SIR6007SF
FDA UDI
Class IIActive
Si SSPAR5055
FDA UDI
Class IIActive
ever GUIDE KIT GFD5004
FDA UDI
Class IActive
Si SAT40
FDA UDI
Class IActive
Si SSA45N20
FDA UDI
Class IIActive
Si NSIR4011SF
FDA UDI
Class IIActive
St STDAW40C
FDA UDI
Class IIActive
evertis TBBCR5045R
FDA UDI
Class IActive
Sinus Kit SKRP42
FDA UDI
Class IActive
Si SIDAN4052
FDA UDI
Class IIActive
Surgical Kit SSD5007A
EUDAMEDFDA UDI
Class IActive
Surgical Kit SBPR65A
FDA UDI
Class IActive
evertis TBBCSR42
FDA UDI
Class IActive
Universal Prosthetic Kit UPK00
FDA UDI
Class IActive
Si SIDAN4556H
FDA UDI
Class IIActive
Sinus Kit SHMLL
FDA UDI
Class IActive
Si SBCR5044H
FDA UDI
Class IActive
Si SSPAR4043
FDA UDI
Class IIActive
Universal Prosthetic Kit UDU00L
FDA UDI
Class IActive
Surgical Kit TWA00
FDA UDI
Class IActive
evertis TBBCS4042R
FDA UDI
Class IActive
Si SFTR60S
FDA UDI
Class IActive
evertis ZTBC35043H
FDA UDI
Class IActive
Si SAA4525N20
EUDAMEDFDA UDI
Class IIActive
evertis TBBCSR45
FDA UDI
Class IActive

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