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The Linden Group Corp

FDA Regulatory Profile

The Linden Group Corp has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 13, 2023 · NAI
Latest 510(k)
Mar 16, 2020

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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
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 13, 2023Cedar Knolls, NJDevicesNo Action Indicated (NAI)3012336461

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
K191705OptikView GUP2103CMIMar 16, 2020
K160328DIVA ZSP2105CMI with QUBYX PerfectLum bundleFeb 25, 2016

FDA data resources