Point Robotics MedTech, Inc.
TaiwanFDA applicant, unverified FDA
- Devices
- 106
- Registrations
- FDA
- FDA recalls
- 0
What Point Robotics MedTech, Inc. makes
Point Robotics MedTech, Inc. makes the POINT Kinguide Agile Hybrid Navigation System and related robotic-assisted surgical systems, including versions with DRF accessories and specific model designations such as PSHF01-000, as well as the POINT Kinguide Agile Robotic Arm Surgical Stereotactic System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Search and filter all 106 devicesDeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
POINT Kinguide Agile Hybrid Navigation System Ref K230087
Regimes: 510(k) Registry: 510(k)POINT Kinguide Robotic-Assisted Surgical System Ref K220241
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Showing 101-106 of 106
Company details
- DUNS number
- 656383289
FDA establishments
- Point Robotics Medtech Inc. Xindian Dist. New Taipei · TW FEI 3021976927