Intraoptics Surgical, Inc.
Country not established
- Devices
- 1
What Intraoptics Surgical, Inc. makes
Intraoptics Surgical, Inc. manufactures phacoemulsifier systems, including the PHACOTRON SYSTEMS PLUS III, designed for cataract surgery to emulsify and aspirate the lens.
The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Phacotron Systems Plus Iii Phacoemulsifier Aspi. Ref K902876
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intraoptics Surgical, Inc. have in the registry?
The registry currently lists 1 device for Intraoptics Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intraoptics Surgical, Inc.'s devices?
Among its 1 most recently registered device, Intraoptics Surgical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intraoptics Surgical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intraoptics Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intraoptics Surgical, Inc. in the registry?
The most recently registered devices listed for Intraoptics Surgical, Inc. include PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI..