Oculeve, Inc.
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Oculeve, Inc. is a medical device manufacturer, with 13 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 13
Registry facts
- Registries
- FDA GUDID 12
- FDA 510(k) 1
- Device classes
- FDA Class II 13
- Identifiers
- DUNS 078797682
What Oculeve, Inc. makes
OCULEVE, INC. manufactures intranasal lacrimal electrical neurostimulators and their associated electrodes, which are devices designed to stimulate tear production via electrical stimulation of nasal nerves. The company also produces reusable electronic device storage covers and noninvasive device battery chargers for use with its neurostimulation system.
The devices manufactured by OCULEVE, INC. are classified as Class II medical devices and are listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system.
Catalogue
Search and filter all 13 devicesCompany details
- DUNS number
- 078797682
- Phone
- +1(415)745-3784
Frequently asked questions
How many devices does OCULEVE, INC. have in the registry?
The registry currently lists 13 devices for OCULEVE, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list OCULEVE, INC.'s devices?
Among its 13 most recently registered devices, OCULEVE, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do OCULEVE, INC.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for OCULEVE, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from OCULEVE, INC. in the registry?
The most recently registered devices listed for OCULEVE, INC. include TrueTear F-0035, TrueTear F-0056, TrueTear F-0059 and TrueTear F-0050.