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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 8 of 25
DeviceModel / ReferenceRegistriesClassStatus
Si STAR4520
FDA UDI
Class IIActive
Sinus Kit SSGK
FDA UDI
Class IActive
Surgical Kit SHS01S
FDA UDI
Class IActive
Si SDAR6074
FDA UDI
Class IIActive
Si STAR4510P
FDA UDI
Class IActive
Si SHAN4070
FDA UDI
Class IIActive
Si SFPUR50S
FDA UDI
Class IActive
Si NSIR4015SF
EUDAMEDFDA UDI
Class IIActive
evertis TBBCS4043R
FDA UDI
Class IActive
Si SDAR5052H
FDA UDI
Class IIActive
Si SSPAA6040
FDA UDI
Class IActive
Surgical Kit TWHA00ES
FDA UDI
Class IActive
Si SIDAN4555H
FDA UDI
Class IIActive
Surgical Kit SBPI62
FDA UDI
Class IActive
Surgical Kit SSD5008A
EUDAMEDFDA UDI
Class IActive
St STBCW6042C
FDA UDI
Class IActive
Si SAA45
FDA UDI
Class IActive
Si SSPAR5042
FDA UDI
Class IIActive
Surgical Kit LLD2313
FDA UDI
Class IActive
Surgical Kit SISK
FDA UDI
Class IActive
Si SSPAR5073
FDA UDI
Class IIActive
Surgical Kit LITD45D
FDA UDI
Class IActive
Si SIR5008SF
FDA UDI
Class IIActive
ever GUIDE KIT GFD4513
FDA UDI
Class IActive
Si SIR7007SF
FDA UDI
Class IIActive
evertis TBBCN5064R
FDA UDI
Class IActive
Short Drill Kit DS50
FDA UDI
Class IActive
Surgical Kit LSD5008
FDA UDI
Class IActive
Si SIDAN5054
FDA UDI
Class IIActive
Si SIDAR4554H
FDA UDI
Class IIActive
Si SBA45R40
FDA UDI
Class IIActive
Si SFTSN00S
FDA UDI
Class IActive
Si SIDAR4556
FDA UDI
Class IIActive
Sm MB2510LR
FDA UDI
Class IIActive
St STW4511LS
FDA UDI
Class IIActive
Si SFTR60HL
FDA UDI
Class IActive
Si SIDAR5052H
FDA UDI
Class IIActive
S-Guide Kit FDW
FDA UDI
Class IActive
Si SSPAA5055
FDA UDI
Class IActive
St STSPAR40
FDA UDI
Class IIActive
Sm MB2508SR
FDA UDI
Class IIActive
Si SBCSN44
FDA UDI
Class IActive
Si NSIN3515S
EUDAMEDFDA UDI
Class IIActive
Si SHAN5020
FDA UDI
Class IIActive
S-Guide Kit TDW3510
FDA UDI
Class IActive
Si SIDAR6045
FDA UDI
Class IIActive
Si SIDAR5041H
FDA UDI
Class IIActive
Si NSIR5011SF
FDA UDI
Class IIActive
St STDAR40C
FDA UDI
Class IIActive
Surgical Kit TWHA00S
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