E.O.S Co., Ltd.
South KoreaFDA 510(k) applicant, unverified FDA FEI 3015369246
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What E.O.S Co., Ltd. makes
E.O.S Co., Ltd. manufactures polymacon soft contact lenses, including tinted and colored variants designed for extended or daily wear. These lenses are formulated with a hydrophilic material to ensure comfort and compatibility with the eye’s natural moisture balance.
The company’s product portfolio is classified under FDA’s Class II medical devices and is listed via the 510(k) premarket notification process. The devices are regulated under US jurisdiction, adhering to FDA requirements for contact lenses.
Catalogue
- 510(k) 510(k)
Company details
- FDA FEI number
- 3015369246
- Address
- 188 Yuram-ro, Dong-gu Daegu
Frequently asked questions
How many devices does E.O.S Co., Ltd. have in the registry?
The registry currently lists 1 device for E.O.S Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list E.O.S Co., Ltd.'s devices?
Among its 1 most recently registered device, E.O.S Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do E.O.S Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for E.O.S Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E.O.S Co., Ltd. in the registry?
The most recently registered devices listed for E.O.S Co., Ltd. include P-CON (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color).