Ocular Innovations, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ocular Innovations, Inc. makes
Ocular Innovations, Inc. manufactures single-use ocular care packs designed for sterile eye irrigation and wound management, including the OCUCARE FREEDOM PACK and OCUCARE PACK. These products are intended for use in clinical settings to provide a sterile solution for flushing the eye or treating ocular surface injuries.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Ocucare Freedom Pack Ref K832559
Regimes: 510(k) Registry: 510(k)Ocucare Pack Ref K830902
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ocular Innovations, Inc. have in the registry?
The registry currently lists 2 devices for Ocular Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ocular Innovations, Inc.'s devices?
Among its 2 most recently registered devices, Ocular Innovations, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ocular Innovations, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ocular Innovations, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ocular Innovations, Inc. in the registry?
The most recently registered devices listed for Ocular Innovations, Inc. include OCUCARE FREEDOM PACK and OCUCARE PACK.