Chiron Intraoptics
Country not established
- Devices
- 4
What Chiron Intraoptics makes
Chiron Intraoptics manufactures ultrasonic handpieces for ophthalmic procedures, including the Phacotron Gold, which integrates multifunctional capabilities for cataract surgery. The company also produces corneal storage media and containers, such as Optisol-GS, Optisol, and modified versions for preserving corneal tissue.
The portfolio includes Class II and unclassified (U) devices, all of which are listed under FDA’s 510(k) pathway. These products are regulated under US medical device laws and are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Dexsol Corneal Storage Media Container, Modified Ref K921728
Regimes: 510(k) Registry: 510(k)Optisol-Gs Corneal Storage Media Ref K924165
Regimes: 510(k) Registry: 510(k)Optisol Corneal Storage Media Container/Modified Ref K921729
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chiron Intraoptics have in the registry?
The registry currently lists 4 devices for Chiron Intraoptics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chiron Intraoptics's devices?
Among its 4 most recently registered devices, Chiron Intraoptics has devices listed in FDA 510(k) (4 devices).
What risk classes do Chiron Intraoptics's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Chiron Intraoptics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chiron Intraoptics in the registry?
The most recently registered devices listed for Chiron Intraoptics include PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECE, DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED, OPTISOL-GS CORNEAL STORAGE MEDIA and OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED.