Kestrel
Country not established
- Devices
- 3
What Kestrel makes
Kestrel manufactures reusable and single-use lens cases designed for storing and transporting contact lenses. These products include standard and specialized cases, such as those with polystyrene inserts for lens protection.
The company’s lens cases are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The devices are listed under the FDA’s 510(k) database.
Catalogue
Kestrel Lens Case 1543-893S/P-1700-2611 Ref K900054
Regimes: 510(k) Registry: 510(k)Kestrel Lens Case 731H-893S/P-1700-2611 Ref K900053
Regimes: 510(k) Registry: 510(k)Kestrel Lens Case (208-12NT Polystyrene) Ref K901748
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kestrel have in the registry?
The registry currently lists 3 devices for Kestrel. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kestrel's devices?
Among its 3 most recently registered devices, Kestrel has devices listed in FDA 510(k) (3 devices).
What risk classes do Kestrel's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Kestrel's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kestrel in the registry?
The most recently registered devices listed for Kestrel include KESTREL LENS CASE 1543-893S/P-1700-2611, KESTREL LENS CASE 731H-893S/P-1700-2611 and KESTREL LENS CASE (208-12NT POLYSTYRENE).