Waypoint Orthopedics, Inc.
Country not established
- Devices
- 2
What Waypoint Orthopedics, Inc. makes
Waypoint Orthopedics, Inc. manufactures the Waypoint GPS, a surgical navigation system designed for orthopedic procedures to enhance precision during joint replacements and bone surgeries.
The company’s portfolio is regulated under FDA Class II devices, with the Waypoint GPS authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Waypoint GPS Ref K222106
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 144837124
Frequently asked questions
How many devices does Waypoint Orthopedics, Inc. have in the registry?
The registry currently lists 2 devices for Waypoint Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Waypoint Orthopedics, Inc.'s devices?
Among its 2 most recently registered devices, Waypoint Orthopedics, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Waypoint Orthopedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Waypoint Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Waypoint Orthopedics, Inc. in the registry?
The most recently registered devices listed for Waypoint Orthopedics, Inc. include Guided Pedicle System (GPS) W101 and Waypoint GPS.