Nexus6, Ltd.
New ZealandFDA applicant, unverified
- Devices
- 2
What Nexus6, Ltd. makes
Nexus6, Ltd. manufactures the SMARTTOUCH, a reusable surgical instrument designed for precision tissue manipulation, and the SMARTTRACK SYSTEM, a real-time tracking solution for surgical tools and implants to enhance procedural accuracy.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. Nexus6, Ltd. is based in the United States and lists its devices in the FDA’s 510(k) registry.
Catalogue
Smarttouch Ref K133951
Regimes: 510(k) Registry: 510(k)Smarttrack System Ref K091803
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nexus6, Ltd. have in the registry?
The registry currently lists 2 devices for Nexus6, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nexus6, Ltd.'s devices?
Among its 2 most recently registered devices, Nexus6, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nexus6, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nexus6, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nexus6, Ltd. in the registry?
The most recently registered devices listed for Nexus6, Ltd. include SMARTTOUCH and SMARTTRACK SYSTEM.