Endorobotics Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Endorobotics Co., Ltd. makes
Endorobotics Co., Ltd. manufactures robotic-assisted surgical systems, including the ROBOPERA (ER-R-002) and ROBOPERA (ER-R-003) devices, designed for minimally invasive laparoscopic procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Robopera (Er-R-002); Robopera (Er-R-003) Ref K244029
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endorobotics Co., Ltd. have in the registry?
The registry currently lists 1 device for Endorobotics Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endorobotics Co., Ltd.'s devices?
Among its 1 most recently registered device, Endorobotics Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Endorobotics Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endorobotics Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endorobotics Co., Ltd. in the registry?
The most recently registered devices listed for Endorobotics Co., Ltd. include ROBOPERA (ER-R-002); ROBOPERA (ER-R-003).