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Patient Pocket, LLC

FDA Regulatory Profile

Patient Pocket, LLC has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 27, 2020 · NAI
Latest 510(k)
Apr 19, 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
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 27, 2020Cherry Hill, NJDevicesNo Action Indicated (NAI)3012335032
Feb 28, 2017Cherry Hill, NJDevicesNo Action Indicated (NAI)3012335032

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
K170215LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDockApr 19, 2017
K152636Laser DockDec 17, 2015

FDA data resources