Data / Medical devices / United States / Visioneering Technologies, Inc
Visioneering Technologies, Inc: FDA-registered device maker in Alpharetta, GA, United States, 3 510(k) clearances
Visioneering Technologies, Inc is registered with the FDA (registration 3010364480) in Alpharetta, GA, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 7, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010364480
- Address
- 4400 N Point Pkwy Ste 265, Alpharetta, GA, United States, 30022
- Owner or operator
- Visioneering Technologies Inc (10047853)
- Roles
- Manufacturer
- First device listed
- November 7, 2014
- Registered through
- 2026
- Brand names listed
- NaturalVue (etafilcon A) 1 Day Contact Lenses, NaturalVue (etafilcon A) Contact Lenses, NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lens, Contact, (Disposable) | MVN | 2 | Manufacturer | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Manufacturer | 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 7, 2017 | K173086 | NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses | LPL | Substantially Equivalent | Visioneering Technologies, Inc. | accessdata.fda.gov |
| April 30, 2015 | K150385 | NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses | LPL | Substantially Equivalent | Visioneering Technologies, Inc. | accessdata.fda.gov |
| October 15, 2014 | K140025 | AQUAMAX (ETAFILCON A) BI-WEEKLY DISPOSABLE SOFT (HYDROPHILIC) CONTACT LENSES | LPL | Substantially Equivalent | Pegavision Corporation | accessdata.fda.gov |
Compare with other makers
Updated November 7, 2017. 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.