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Saving Sight

FDA Regulatory Profile

Saving Sight has 0 FDA recalls, 19 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 25, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections19Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 25, 2026Kansas City, MOBiologicsNo Action Indicated (NAI)3003347229
Aug 6, 2025Springfield, MOBiologicsNo Action Indicated (NAI)3001238378
Jun 12, 2024Columbia, MOBiologicsNo Action Indicated (NAI)3003153264
Sep 19, 2018Kansas City, MOBiologicsNo Action Indicated (NAI)3003347229
Jun 13, 2018Columbia, MOBiologicsNo Action Indicated (NAI)3003153264
Mar 8, 2018Springfield, MOBiologicsNo Action Indicated (NAI)3001238378
May 10, 2016Hutchinson, KSBiologicsNo Action Indicated (NAI)3009083358
Apr 21, 2016Kansas City, MOBiologicsNo Action Indicated (NAI)3003347229
Dec 17, 2015Springfield, MOBiologicsNo Action Indicated (NAI)3001238378
Oct 27, 2015Columbia, MOBiologicsNo Action Indicated (NAI)3003153264
Sep 19, 2014Springfield, MOBiologicsNo Action Indicated (NAI)3001238378
Feb 19, 2014Kansas City, MOBiologicsVoluntary Action Indicated (VAI)3003347229
Jan 15, 2014Columbia, MOBiologicsNo Action Indicated (NAI)3003153264
Jan 2, 2014Hutchinson, KSBiologicsNo Action Indicated (NAI)3009083358
May 16, 2012Hutchinson, KSBiologicsNo Action Indicated (NAI)3009083358
Apr 18, 2012Kansas City, MOBiologicsNo Action Indicated (NAI)3003347229
Apr 5, 2010Kansas City, MOBiologicsNo Action Indicated (NAI)3003347229
Mar 30, 2010Springfield, MOBiologicsVoluntary Action Indicated (VAI)3001238378
Feb 3, 2010Columbia, MOBiologicsNo Action Indicated (NAI)3003153264

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3003347229Kansas City, MO6Feb 25, 2026
FEI 3001238378Springfield, MO5Aug 6, 2025
FEI 3003153264Columbia, MO5Jun 12, 2024
FEI 3009083358Hutchinson, KS3May 10, 2016

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.