Optikon Oftalmologia SpA
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- Devices
- 1
What Optikon Oftalmologia SpA makes
Optikon Oftalmologia Spa manufactures the PERIKON PCL 90, a device designed for ophthalmological procedures, specifically for corneal cross-linking to treat keratoconus and other corneal ectasias.
The PERIKON PCL 90 is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Perikon Pcl 90 Ref K922294
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Optikon Oftalmologia Spa have in the registry?
The registry currently lists 1 device for Optikon Oftalmologia Spa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Optikon Oftalmologia Spa's devices?
Among its 1 most recently registered device, Optikon Oftalmologia Spa has devices listed in FDA 510(k) (1 device).
What risk classes do Optikon Oftalmologia Spa's devices fall under?
Among its 1 most recently registered device, the classes recorded for Optikon Oftalmologia Spa's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Optikon Oftalmologia Spa in the registry?
The most recently registered devices listed for Optikon Oftalmologia Spa include PERIKON PCL 90.