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U.S. Iol, Inc.

FDA Regulatory Profile

U.S. Iol, Inc. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Sep 19, 2000

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances4Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Us Iol
Same company group		0050—

Recent 510(k) Clearances

K-NumberDeviceDate
K001768OCCU-FLO PUNCTUM PLUGSSep 19, 2000
K954746PHACO TIPJan 11, 1996
K954239U.S. IOL PHACO HANDPIECEDec 8, 1995
K954240EVOLUTION PHACOMULSIFIERDec 1, 1995

FDA data resources

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