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SurgiCore Co., Ltd.

South Korea KR-MF-000032606 Last updated 21 Oct 2026

Devices
16
Registries
EUDAMED
FDA recalls
0

Catalogue16

Authorised representatives

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.

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 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.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
South Korea
Address
Bldg. A, D, 43-10, Jingoksandan 5beon-ro, Gwangju, South Korea
Phone
+82 62 714 3850
PRRC contact
SEUNGMIN LEE
EUDAMED SRN
KR-MF-000032606