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Visioneering Technologies, Inc.

FDA Regulatory Profile

Visioneering Technologies, Inc. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 9, 2015 · NAI
Latest 510(k)
Nov 7, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 9, 2015Alpharetta, GADevicesNo Action Indicated (NAI)3010364480

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K173086NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact LensesNov 7, 2017
K150385NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact LensesApr 30, 2015

FDA data resources