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Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG

FDA Regulatory Profile

Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Feb 10, 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) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K190192K3Pro Konus New Abutments and ImplantsFeb 10, 2020
K160581K3PRO Konus Additional Abutments and ImplantsMar 24, 2017
K160574K3PRO SURGICAL TRAYDec 20, 2016

FDA data resources