SurgiCore Co., Ltd.
South Korea KR-MF-000032606 Last updated 21 Oct 2026
- Devices
- 16
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SurgiTractor Ref ST0509
ThePort Ref TP05-100DC
SurgiTractor Ref ST0914
SurgiTractor Ref STC0306
SurgiTractor Ref ST1117
SurgiTractor Ref ST0103
ThePort Ref TP05-75DC
ThePort Ref TP10-75
SurgiTractor Ref ST0204
ThePort Ref TP12-75
SurgiTractor Ref ST0306KB
SurgiTractor Ref ST0306
SurgiTractor Ref ST0306K
ThePort Ref TP10-150
ThePort Ref TP12-150
SurgiTractor Ref ST1725
Related companies
Authorised representatives
- Obelis s.a. BE
What SurgiCore Co., Ltd. makes
SurgiCore Co., Ltd. manufactures surgical robotic systems, including the SurgiTractor, which is designed for minimally invasive procedures to assist in tissue manipulation and precision positioning during operations. The company also produces laparoscopic port devices, known as ThePort, used for creating access points in minimally invasive surgeries to introduce surgical instruments and cameras into the abdominal or thoracic cavity.
The company’s devices are classified under EU Medical Device Regulation as Class IIa and are registered in the EU’s eudamed database. SurgiCore Co., Ltd. is headquartered in South Korea.
Frequently asked questions
What types of medical devices does SurgiCore Co., Ltd. manufacture?
SurgiCore Co., Ltd. specializes in surgical robotic systems and laparoscopic port devices. Their SurgiTractor is a robotic system designed for minimally invasive procedures, assisting with tissue manipulation and precision positioning during surgery. Additionally, they produce ThePort, a laparoscopic port device used to create access points for surgical instruments and cameras in minimally invasive abdominal or thoracic procedures.
Where is SurgiCore Co., Ltd. based, and what is its primary focus?
SurgiCore Co., Ltd. is headquartered in South Korea. The company focuses on developing advanced surgical tools for minimally invasive procedures, including robotic-assisted systems and laparoscopic ports, to improve precision and reduce surgical invasiveness.
Which regulatory registries list SurgiCore Co., Ltd.’s devices?
SurgiCore Co., Ltd.’s devices are listed in the eudamed database, which is the EU’s central registry for medical devices. This registry is used to track and monitor devices authorized under the EU Medical Device Regulation (MDR).
How are SurgiCore Co., Ltd.’s devices classified under EU regulations?
Under the EU Medical Device Regulation (MDR), SurgiCore Co., Ltd.’s devices are classified as Class IIa. This classification is determined based on factors like the device’s intended purpose, risk level, and potential impact on patient safety, with Class IIa representing a moderate risk category requiring compliance with specific regulatory requirements.
Information
- Country
- South Korea
- Address
- Bldg. A, D, 43-10, Jingoksandan 5beon-ro, Gwangju, South Korea
- Website
- www.surgicore.co.kr
- [email protected]
- Phone
- +82 62 714 3850
- PRRC contact
- SEUNGMIN LEE
- EUDAMED SRN
- KR-MF-000032606