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Ncs Lab Srl

FDA Regulatory Profile

Ncs Lab Srl has 0 FDA recalls, 1 inspection, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 12, 2024 · NAI
Latest 510(k)
Oct 14, 2022

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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) clearances4Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 12, 2024Carpi, ItalyDevicesNo Action Indicated (NAI)3011410128

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
K220994Shoulder PacemakerTMOct 14, 2022
K210674Shoulder PacemakerAug 24, 2021
K160500Elite SPK, Compasso, Elite SPK KitApr 20, 2016
K120356NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MDDec 11, 2012

FDA data resources