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ZiphyCare, Inc.

FDA Regulatory Profile

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

Latest inspection
Jul 30, 2025 · VAI

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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
Inspections4Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 30, 2025New York, NYDevicesVoluntary Action Indicated (VAI)3011682748
Sep 6, 2022New York, NYDevicesVoluntary Action Indicated (VAI)3011682748
Oct 25, 2018New York, NYDevicesVoluntary Action Indicated (VAI)3011682748
Nov 2, 2015New York, NYDevicesVoluntary Action Indicated (VAI)3011682748

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 3011682748New York, NY4Jul 30, 2025

FDA data resources

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