Visioneering Technologies, Inc. is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visioneering Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses, NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses
2
Total
2
Cleared
0
Denied
Visioneering Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Visioneering Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regsolutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Visioneering Technologies, Inc.
2 devices