Data / Medical devices / China / Shenzhen Lensgoo Vision Co., Ltd.
Shenzhen Lensgoo Vision Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Lensgoo Vision Co., Ltd. is registered with the FDA (registration 3039456814) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 2, 2011. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3039456814
- Address
- Unit 201, Building No. 69, Dayun Software Town, No. 8288 Longgang Boulevard, Longgang, Shenzhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Lensgoo Vision Co., Ltd. (10093775)
- Roles
- Repackager or relabeler
- First device listed
- July 8, 2025
- Registered through
- 2026
- Brand names listed
- Freshgo, SEE CLEAR SOFT CONTACT LENS, SEE CLEAR COLOR SOFT CONTACT LENS, FIERCE SOFT CONTACT LENS, SEE CLEAR 38;, Magister, SEE CLEAR SOFT CONTACT LENS, SEE CLEAR COLOR SOFT CONTACT LENS, FIERCE SOFT CONTACT LENS, SEE CLEAR 38;, Pseyeche, SEE CLEAR SOFT CONTACT LENS, SEE CLEAR COLOR SOFT CONTACT LENS, FIERCE SOFT CONTACT LENS, SEE CLEAR 38;
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 2, 2011 | K111345 | SEE CLEAR SOFT CONTACT LENS, SEE CLEAR COLOR SOFT CONTACT LENS, FIERCE SOFT CONTACT LENS | LPL | Substantially Equivalent | The See Clear Company, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 2, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.