The See Clear Company, Inc.
Country not established
- Devices
- 1
- FDA recalls
- 10 ongoing since 2021 (1 open in total)
At a glance
Market reach
- United States
- FDA recalls
What The See Clear Company, Inc. makes
The See Clear Company, Inc. manufactures soft contact lenses, including clear, colored, and tinted variants designed for vision correction and cosmetic use.
These products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
See Clear Soft Contact Lens, See Clear Color Soft Contact Lens, Fierce Soft Contact Lens Ref K111345
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by The See Clear Company, Inc., initiated on 2017-01-06. By recorded status: 1 ongoing. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 1
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2017
- 6 Jan 2017 Z-1404-2017 Class II Open since 2017 Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.
Full distribution text
- 6 Jan 2017 Z-1404-2017 Class II Open since 2017 Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.
Frequently asked questions
How many devices does The See Clear Company, Inc. have in the registry?
The registry currently lists 1 device for The See Clear Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The See Clear Company, Inc.'s devices?
Among its 1 most recently registered device, The See Clear Company, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The See Clear Company, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The See Clear Company, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for The See Clear Company, Inc.?
FDA recall records list 1 recall initiated by The See Clear Company, Inc., the most recent initiated on 6 Jan 2017. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from The See Clear Company, Inc. in the registry?
The most recently registered devices listed for The See Clear Company, Inc. include SEE CLEAR SOFT CONTACT LENS, SEE CLEAR COLOR SOFT CONTACT LENS, FIERCE SOFT CONTACT LENS.