Saint John'S Plaza Medical Group
Country not established
- Devices
- 1
What Saint John'S Plaza Medical Group makes
Saint John's Plaza Medical Group manufactures phacosurgical systems, including phacosopes designed for cataract surgery procedures. These devices facilitate the removal of the eye’s natural lens through phacoemulsification techniques, a common approach in ophthalmic interventions.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry, adhering to US medical device regulations.
Catalogue
Phacoscope Ref K960811
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Saint John'S Plaza Medical Group have in the registry?
The registry currently lists 1 device for Saint John'S Plaza Medical Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Saint John'S Plaza Medical Group's devices?
Among its 1 most recently registered device, Saint John'S Plaza Medical Group has devices listed in FDA 510(k) (1 device).
What risk classes do Saint John'S Plaza Medical Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Saint John'S Plaza Medical Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Saint John'S Plaza Medical Group in the registry?
The most recently registered devices listed for Saint John'S Plaza Medical Group include PHACOSCOPE.