Escalon Medical Corp.

FDA Regulatory Profile

Escalon Medical Corp. has 0 FDA recalls, 4 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 5, 2025 · NAI
Latest 510(k)
Dec 23, 2009

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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) clearances3Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 5, 2025New Berlin, WIDevicesNo Action Indicated (NAI)2183477
Nov 25, 2019New Berlin, WIDevicesVoluntary Action Indicated (VAI)2183477
Mar 7, 2013New Berlin, WIDevicesVoluntary Action Indicated (VAI)2183477
Apr 12, 2010New Berlin, WIDevicesNo Action Indicated (NAI)2183477

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 2183477New Berlin, WI4Aug 5, 2025

Recent 510(k) Clearances

K-NumberDeviceDate
K093613VASCUVIEW TAP ULTRASOUND SYSTEMDec 23, 2009
K080049VASCUVIEW ULTRASOUND SYSTEMJan 23, 2008
K002920MEGAVISION CPX, MEGAVISION FA, MODEL I AND IIDec 18, 2000

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