I-Codi Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What I-Codi Co., Ltd. makes
I-Codi Co., Ltd. manufactures Giselle (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses, available in clear and tinted variants. These are designed for single-use, disposable daily wear and are intended for vision correction.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does I-Codi Co., Ltd. have in the registry?
The registry currently lists 1 device for I-Codi Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I-Codi Co., Ltd.'s devices?
Among its 1 most recently registered device, I-Codi Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do I-Codi Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for I-Codi Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from I-Codi Co., Ltd. in the registry?
The most recently registered devices listed for I-Codi Co., Ltd. include Giselle (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted).