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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 16 of 25
DeviceModel / ReferenceRegistriesClassStatus
St STW4507SSF
FDA UDI
Class IIActive
Si SSA55R10
FDA UDI
Class IIActive
Sinus Kit SHSC
FDA UDI
Class IActive
Si SDAR4542
FDA UDI
Class IIActive
Si SDAR4574H
FDA UDI
Class IIActive
Si SDAN5044
FDA UDI
Class IIActive
Si SIDAR4554
FDA UDI
Class IIActive
Se EBCN5042H
FDA UDI
Class IActive
Si STC55BP
FDA UDI
Class IActive
Surgical Kit LLD2311
FDA UDI
Class IActive
Se EBCN5066H
FDA UDI
Class IActive
Si SSPBC45S
FDA UDI
Class IActive
Surgical Kit SBPW62
FDA UDI
Class IActive
Surgical Kit TWBAA00
FDA UDI
Class IActive
Si SAPUS18
FDA UDI
Class IActive
St STAGAW15C
FDA UDI
Class IIActive
Si SBCSR65
FDA UDI
Class IActive
Surgical Kit LSD5013
FDA UDI
Class IActive
St STR4511LSF
FDA UDI
Class IIActive
Si SDAR4542H
FDA UDI
Class IIActive
Repair Kit SRK00
FDA UDI
Class IActive
Sinus Kit SSCA00
FDA UDI
Class IActive
Surgical Kit SSD3511A
EUDAMEDFDA UDI
Class IActive
Si SDAR5053H
FDA UDI
Class IIActive
Short Drill Kit LCB50S
FDA UDI
Class IActive
St STBCR5041C
FDA UDI
Class IActive
Si SBA45R60
FDA UDI
Class IIActive
evertis TBBCSS44
FDA UDI
Class IActive
Surgical Kit LCB60
FDA UDI
Class IActive
evertis NSSD3507
FDA UDI
Class IActive
Se EBCSR64
FDA UDI
Class IActive
Si SIDAN5053
FDA UDI
Class IIActive
Si STAN4030P
FDA UDI
Class IActive
St STR4510SSF
FDA UDI
Class IIActive
Surgical Kit SSD2008A
FDA UDI
Class IActive
evertis NSSD4007
FDA UDI
Class IActive
Si SSA55R30
FDA UDI
Class IIActive
St STR4011SS
FDA UDI
Class IIActive
Si SIDAN4551
FDA UDI
Class IIActive
Si SFPUR60HL
FDA UDI
Class IActive
Surgical Kit SBPN42
FDA UDI
Class IActive
St STBCSW42
FDA UDI
Class IActive
Surgical Kit TWFA01RS
FDA UDI
Class IActive
Short Drill Kit SSD2004
FDA UDI
Class IActive
Surgical Kit SSD5011A
EUDAMEDFDA UDI
Class IActive
Si SDAR6044H
FDA UDI
Class IIActive
St STSPAR70
FDA UDI
Class IIActive
Repair Kit RKSLGR
FDA UDI
Class IActive
Surgical Kit TWFA00NL
FDA UDI
Class IActive
Si SSPBC40S
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