Evolution Optiks Limited
BarbadosFDA 510(k) applicant, unverified
- Devices
- 1
What Evolution Optiks Limited makes
Evolution Optiks Limited manufactures the LFR-260, a Class I laser-based device designed for specific ophthalmic applications, including low-level retinal treatments.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the United States. The manufacturer is based in the US.
Catalogue
Lfr-260 Ref K233295
510(k) 510(k)
Frequently asked questions
How many devices does Evolution Optiks Limited have in the registry?
The registry currently lists 1 device for Evolution Optiks Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Evolution Optiks Limited's devices?
Among its 1 most recently registered device, Evolution Optiks Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Evolution Optiks Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Evolution Optiks Limited's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Evolution Optiks Limited in the registry?
The most recently registered devices listed for Evolution Optiks Limited include LFR-260.