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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 12 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si SDAR6075H
FDA UDI
Class IIActive
Si SSPAR4044
FDA UDI
Class IIActive
Surgical Kit SSD4011A
EUDAMEDFDA UDI
Class IActive
St STCTAR40
FDA UDI
Class IIActive
S-Guide Kit NMDM
FDA UDI
Class IActive
ever GUIDE KIT GFD3511
FDA UDI
Class IActive
Si SIDAR5056
FDA UDI
Class IIActive
ever GUIDE KIT GCB35
FDA UDI
Class IActive
Sinus Kit SIST07
FDA UDI
Class IActive
Si SDAR6073
FDA UDI
Class IIActive
Universal Prosthetic Kit UDH20S
FDA UDI
Class IActive
evertis ZTBC56043H
FDA UDI
Class IActive
Si SIR4513SF
FDA UDI
Class IIActive
Si NSIR5007SF
FDA UDI
Class IIActive
Si SIDAR5072
FDA UDI
Class IIActive
Si SSPAR4544
FDA UDI
Class IIActive
Si SAA4515N40HF
FDA UDI
Class IIActive
Sinus Kit SHMLS
FDA UDI
Class IActive
Si SIDAN4554
FDA UDI
Class IIActive
evertis TTBCR5062C
FDA UDI
Class IActive
evertis NSSD5015
FDA UDI
Class IActive
Si SPP45
FDA UDI
Class IActive
St STR3513SS
FDA UDI
Class IIActive
Surgical Kit SHS00L
FDA UDI
Class IActive
S-Guide Kit HGS57
FDA UDI
Class IActive
S-Guide Kit TDW5010
FDA UDI
Class IActive
Si STAR5020P
FDA UDI
Class IActive
Surgical Kit SBPR62
FDA UDI
Class IActive
Si NSIR4013S
FDA UDI
Class IIActive
Surgical Kit HFD00RL
FDA UDI
Class IActive
evertis TTBCN5031R
FDA UDI
Class IActive
Surgical Kit SSD2010A
FDA UDI
Class IActive
Surgical Kit SSD4007A
EUDAMEDFDA UDI
Class IActive
Si SIDAN5053H
FDA UDI
Class IIActive
Surgical Kit SHS01ES
FDA UDI
Class IActive
Si SICAR5515
FDA UDI
Class IIActive
St STCTAR20
FDA UDI
Class IIActive
Si SDAR6053H
FDA UDI
Class IIActive
Sm MB3011LR
FDA UDI
Class IIActive
S-Guide Kit TDR4585
FDA UDI
Class IActive
St STAGAW15
FDA UDI
Class IIActive
Si SICAN4015H
FDA UDI
Class IIActive
St STBCW6062C
FDA UDI
Class IActive
S-Guide Kit DE10
FDA UDI
Class IActive
Si SBA45R30
FDA UDI
Class IIActive
Si SDAN5074
FDA UDI
Class IIActive
Se EBCSN64
FDA UDI
Class IActive
Si STAN4030HP
FDA UDI
Class IActive
Si STC45S
FDA UDI
Class IIActive
Si SIDAR4557H
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