Medjet, Inc.
Country not established
- Devices
- 1
What Medjet, Inc. makes
Medjet, Inc. manufactures the HydroBrush™ Keratome, a device used for corneal sculpting in refractive surgery procedures, such as laser-assisted in situ keratomileusis (LASIK) or photorefractive keratectomy (PRK).
The HydroBrush™ Keratome 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
Hydrobrush (Tm) Keratome Ref K971078
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medjet, Inc. have in the registry?
The registry currently lists 1 device for Medjet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medjet, Inc.'s devices?
Among its 1 most recently registered device, Medjet, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medjet, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medjet, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medjet, Inc. in the registry?
The most recently registered devices listed for Medjet, Inc. include HYDROBRUSH (TM) KERATOME.