Dreamcon Co., Ltd.
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Dreamcon Co., Ltd. makes
Dreamcon Co., Ltd. manufactures soft, hydrophilic contact lenses, including the DREAM COLOR I and DREAM COLOR II (POLYMACON) series, designed for daily or extended wear.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- 510(k) 510(k)
FDA establishments
- DreamCon Co. Ltd. Yangsan-si Gyeongnam · KR FEI 3010460316
Frequently asked questions
How many devices does Dreamcon Co., Ltd. have in the registry?
The registry currently lists 1 device for Dreamcon Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dreamcon Co., Ltd.'s devices?
Among its 1 most recently registered device, Dreamcon Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dreamcon Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dreamcon Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dreamcon Co., Ltd. in the registry?
The most recently registered devices listed for Dreamcon Co., Ltd. include DREAM COLOR I (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, DREAM COLOR II (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, D.
Which FDA establishments are linked to Dreamcon Co., Ltd.?
1 FDA establishment is linked to Dreamcon Co., Ltd. in the registry; they are listed on the company page.