Oasis
Country not established
- Devices
- 2
What Oasis makes
Oasis manufactures disposable H-PE microkeratome blades for ophthalmic procedures, as well as ENT (ear, nose, and throat) packings, wicks, wipes, and sponges designed for single-use medical applications.
These products are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Disposable H-Pe Microkeratome Blades Ref K001464
Regimes: 510(k) Registry: 510(k)Ent Packings, Wicks, Wipes, And Sponges Ref K954449
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oasis have in the registry?
The registry currently lists 2 devices for Oasis. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oasis's devices?
Among its 2 most recently registered devices, Oasis has devices listed in FDA 510(k) (2 devices).
What risk classes do Oasis's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oasis's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Oasis in the registry?
The most recently registered devices listed for Oasis include DISPOSABLE H-PE MICROKERATOME BLADES and ENT PACKINGS, WICKS, WIPES, AND SPONGES.