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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 23 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SDAR6042
FDA UDI
Class IIActive
evertis TBBCR5065R
FDA UDI
Class IActive
Si SSPAA5040
FDA UDI
Class IActive
Si SIDAR5077
FDA UDI
Class IIActive
Surgical Kit SSD3515A
EUDAMEDFDA UDI
Class IActive
Si SDAN4551
FDA UDI
Class IIActive
Si NSHAN4546
FDA UDI
Class IIActive
Si SBCSR44
FDA UDI
Class IActive
Si SDAR6071
FDA UDI
Class IIActive
evertis ZTBC35042H
FDA UDI
Class IActive
Surgical Kit SBPN50
FDA UDI
Class IActive
Surgical Kit LLD2310
FDA UDI
Class IActive
Surgical Kit LSD4010
FDA UDI
Class IActive
evertis TTBCR5042C
FDA UDI
Class IActive
Surgical Kit SMH01
FDA UDI
Class IActive
Sinus Kit SIDR20
FDA UDI
Class IActive
Si SSPAN4551
FDA UDI
Class IIActive
Si SSPAR4572
FDA UDI
Class IIActive
evertis ZTBC45043H
FDA UDI
Class IActive
Surgical Kit LSD4511
FDA UDI
Class IActive
Sinus Kit SHSC3
FDA UDI
Class IActive
Si SIDAR5057
FDA UDI
Class IIActive
Si SSPAR4542
FDA UDI
Class IIActive
Si SSPAR4551
FDA UDI
Class IIActive
Si SIDAR5051
FDA UDI
Class IIActive
Si SSPBC60B
FDA UDI
Class IActive
ever GUIDE KIT GFDHR
FDA UDI
Class IActive
evertis NSSD5007
FDA UDI
Class IActive
evertis ZTBCS65
FDA UDI
Class IActive
Si SIR5013S
FDA UDI
Class IIActive
Si SIDAN4055
FDA UDI
Class IIActive
Si STAR4530P
FDA UDI
Class IActive
Si NSIR7008SF
FDA UDI
Class IIActive
Si SIDAN4054
FDA UDI
Class IIActive
Si SHAN5520
FDA UDI
Class IIActive
Si SSPAR4072
FDA UDI
Class IIActive
Si SIDAN4553
FDA UDI
Class IIActive
Si SIDAN4551H
FDA UDI
Class IIActive
St STCSRL
FDA UDI
Class IIActive
ever GUIDE KIT GLD2610
FDA UDI
Class IActive
St STBCR5062C
FDA UDI
Class IActive
ever GUIDE KIT EGK
FDA UDI
Class IActive
Surgical Kit LSD5010
FDA UDI
Class IActive
Si SDAR6054H
FDA UDI
Class IIActive
Surgical Kit SISK03U
FDA UDI
Class IActive
Si SPP55
FDA UDI
Class IActive
Si SSPAR4552
FDA UDI
Class IIActive
Si SSPAC60
FDA UDI
Class IActive
S-Guide Kit TDR4513
FDA UDI
Class IActive
Si SHAR5550
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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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