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Kurin, Inc.

FDA Regulatory Profile

Kurin, Inc. has 0 FDA recalls, 1 inspection, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 27, 2022 · NAI
Latest 510(k)
Apr 28, 2023

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 27, 2022San Diego, CADevicesNo Action Indicated (NAI)3013696225

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
K220677Kurin Blood Culture Collection Set with Kurin Lock TechnologyApr 28, 2023
K191832Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models…Feb 4, 2020
K181895Kurin PIV Blood Collection Set with High PressureJan 18, 2019

FDA data resources