Dws S.R.L.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What Dws S.R.L. makes
Dws S.R.L. manufactures the Temporis and Irix Plus, which are medical devices designed for ophthalmic use, likely including intraocular lenses or related surgical implants.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Temporis, Irix Plus Ref K231142
510(k) 510(k)
Frequently asked questions
How many devices does Dws S.R.L. have in the registry?
The registry currently lists 1 device for Dws S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dws S.R.L.'s devices?
Among its 1 most recently registered device, Dws S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Dws S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dws S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dws S.R.L. in the registry?
The most recently registered devices listed for Dws S.R.L. include Temporis, Irix Plus.