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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 24 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si STC55S
FDA UDI
Class IIActive
Si SIDAN4557H
FDA UDI
Class IIActive
Si STAR4530H
FDA UDI
Class IIActive
Se EBCSW42
FDA UDI
Class IActive
St STBCR5042C
FDA UDI
Class IActive
Si SIDAN4556
FDA UDI
Class IIActive
Surgical Kit LITD50D
FDA UDI
Class IActive
Si NSHAR4534
FDA UDI
Class IIActive
Surgical Kit BCD14
FDA UDI
Class IActive
Surgical Kit HFD00REL
FDA UDI
Class IActive
Si NSHAR5033
FDA UDI
Class IIActive
Surgical Kit LSD3515
FDA UDI
Class IActive
St STW5008SS
EUDAMEDFDA UDI
Class IIActive
St STCLSR
FDA UDI
Class IIActive
Si SIDAR6044H
FDA UDI
Class IIActive
Se EBCSN42
FDA UDI
Class IActive
Si SBCR5045H
FDA UDI
Class IActive
Surgical Kit SSD3513A
EUDAMEDFDA UDI
Class IActive
Si SSPAR4051
FDA UDI
Class IIActive
evertis TBBCR5066R
FDA UDI
Class IActive
Si SPP40
FDA UDI
Class IActive
S-Guide Kit TDW4585
FDA UDI
Class IActive
Si SDAN4575H
FDA UDI
Class IIActive
Sm MB3013SR
FDA UDI
Class IIActive
St STBCSR31
FDA UDI
Class IActive
Si SSA55R50
FDA UDI
Class IIActive
ever GUIDE KIT GMDH
FDA UDI
Class IActive
Si NSHAR4523
FDA UDI
Class IIActive
ever GUIDE KIT GFD4507
FDA UDI
Class IActive
Si SIDAR5051H
FDA UDI
Class IIActive
Si SHAR6035
FDA UDI
Class IIActive
Surgical Kit SDE00
FDA UDI
Class IActive
Si SIN3510SF
FDA UDI
Class IIActive
evertis TBBCR5042R
FDA UDI
Class IActive
Sinus Kit ST32
FDA UDI
Class IActive
Si SAA5525R40H
FDA UDI
Class IIActive
Si SIR7010S
FDA UDI
Class IIActive
evertis NSSD4015
FDA UDI
Class IActive
Si SIDAR5076H
FDA UDI
Class IIActive
Si SDAN4573H
FDA UDI
Class IIActive
Sinus Kit SIDR2802
FDA UDI
Class IActive
Sinus Kit SKRP32
FDA UDI
Class IActive
Si STAR4520HP
FDA UDI
Class IActive
Si SIDAR4552
FDA UDI
Class IIActive
St STR3513SSF
FDA UDI
Class IIActive
Si SIN3511S
FDA UDI
Class IIActive
Si SIR6008SF
FDA UDI
Class IIActive
Surgical Kit HFD00NL
FDA UDI
Class IActive
evertis TBBCN5066R
FDA UDI
Class IActive
Sm MB2513SR
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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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