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Artventive Medical Group, Inc.

FDA Regulatory Profile

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

Latest inspection
Feb 1, 2024 · NAI
Latest 510(k)
Mar 1, 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) clearances3Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 1, 2024San Marcos, CADevicesNo Action Indicated (NAI)3010606221

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
K212057Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOSMar 1, 2022
K150402Endoluminal Occlusion System-EOSSep 25, 2015
K133924ENDOLUMINAL OCCLUSION SYSTEM (EOS)Dec 3, 2014

FDA data resources