Artoss GmbH

FDA Regulatory Profile

Artoss GmbH has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 23, 2019

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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
K190110NanoBone SBX PUTTY, NanoBone QDApr 23, 2019
K161351NanoBone SBX PuttyOct 26, 2016
K141189NANOBONE / GRANULATEJan 30, 2015