Ophthalmic Solution Inc.
United Statesfrom the FDA registration address FDA FEI 3007207818
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3007207818
- Address
- 820 Corridor Park Blvd, Knoxville, TN, 37932
- Website
- ophthalmicsolutioninc.com/
- [email protected]
- Phone
- 18656714300
From the company website
Partner with Ophthalmic Solutions Inc. (OSI) as a trusted OEM manufacturer offering customized, high-precision IOL designs using advanced hydrophobic and hydrophilic acrylic materials. Leverage our expertise to build your brand with superior optical quality. Contact us today to discuss OEM partnership opportunities.
Frequently asked questions
How many devices does Ophthalmic Solution Inc. have in the registry?
The registry currently lists 2 devices for Ophthalmic Solution Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ophthalmic Solution Inc.'s devices?
Among its 2 most recently registered devices, Ophthalmic Solution Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do Ophthalmic Solution Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ophthalmic Solution Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Ophthalmic Solution Inc. in the registry?
The most recently registered devices listed for Ophthalmic Solution Inc. include Intraocular Lens.