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Trident S.R.L

FDA Regulatory Profile

Trident S.R.L has 0 FDA recalls, 1 inspection, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 8, 2023 · NAI
Latest 510(k)
Jul 10, 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) clearances5Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 8, 2023Castenedolo, ItalyDevicesNo Action Indicated (NAI)3012649815

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
K222666X-View 3D Pan/X-View 2D PanJul 10, 2023
K200625I-View Gold and Imagen Gold Dental SensorsApr 15, 2020
K182206RiX70 DCSep 13, 2018
K162619I View and Imagen SensorNov 4, 2016
K160386ReadeR, VieweR, QuickScan PSPMar 10, 2016

FDA data resources