Data / Medical devices / United Kingdom / E-Vision Advisors Ltd
E-Vision Advisors Ltd: FDA-registered device maker in STAINES Surrey, United Kingdom, 6 510(k) clearances
E-Vision Advisors Ltd is registered with the FDA (registration 3035385765) in STAINES Surrey, United Kingdom. It lists 2 device types. The FDA files 6 510(k) clearances under its listings, the newest dated June 2, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035385765
- Address
- 50 Shortwood Avenue, STAINES Surrey, United Kingdom, TW184JL
- Owner or operator
- E-VISION ADVISORS LTD (10092534)
- Roles
- Exporter to the US
- First device listed
- January 17, 2025
- Registered through
- 2026
- Brand names listed
- 1 Day Acuvue Moist; 1 Day Acuvue Moist for Astigmatism; Acuvue oasys for astigmatism, Acuvue vita (6pack), Acuvue vita Toric (6pack), Acuvue2 6 Pack, BioTrue One Day Astigmatism DW contact lenses, FreshLook ColorBlends 2 pack, ULTRA one day 90 PACK
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lens, Contact, (Disposable) | MVN | 2 | Exporter to the US | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| June 2, 2020 | K200528 | Bausch + Lomb (Kalifilcon A) Soft Contact Lens, Bausch + Lomb (Kalifilcon A) Soft Contact Lens for astigmatism | LPL | Substantially Equivalent | Bausch + Lomb, Incorporated | accessdata.fda.gov |
| August 3, 2018 | K181796 | FreshLook Handling Tint, FreshLook Colors, FreshLook ColorBlends, FreshLook Dimensions | LPL | Substantially Equivalent | Alcon Laboratories, Inc. | accessdata.fda.gov |
| March 28, 2016 | K160212 | ACUVUE (senofilcon C) Soft Contact Lens | LPL | Substantially Equivalent | Johnson & Johnson Vision Care, Inc. | accessdata.fda.gov |
| February 13, 2015 | K143632 | Bausch + Lomb Biotrue ONEday for Astigmatism(nesofilcon A) Soft (hydrophilic) Contact Lens | LPL | Substantially Equivalent | Bausch & Lomb, Incorporated | accessdata.fda.gov |
| November 1, 2006 | K062614 | VISTAKON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS, CLEAR AND TINTED (VISIBILITY AND/OR COSMETICALLY) | LPL | Substantially Equivalent | Johnson & Johnson Vision Care, Inc. | accessdata.fda.gov |
| October 28, 2004 | K042275 | VISTAKON (SENOFILCON A) SOFT CONTACT LENS | LPL | Substantially Equivalent | Vistakon | accessdata.fda.gov |
Compare with other makers
Updated June 2, 2020. 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.