Hypervision Surgical
United KingdomFDA applicant, unverified
- Devices
- 1
What Hypervision Surgical makes
Hypervision Surgical manufactures the HyperSnap Surgical System (HSS), a device designed for intraoperative imaging and documentation of surgical procedures, enabling real-time capture and storage of surgical views.
The company’s portfolio is regulated under FDA Class II devices, with the HyperSnap Surgical System authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
HyperSnap Surgical System (HSS) Ref K250268
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hypervision Surgical have in the registry?
The registry currently lists 1 device for Hypervision Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hypervision Surgical's devices?
Among its 1 most recently registered device, Hypervision Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Hypervision Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hypervision Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hypervision Surgical in the registry?
The most recently registered devices listed for Hypervision Surgical include HyperSnap Surgical System (HSS).