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Ergoline GmbH

FDA Regulatory Profile

Ergoline GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 15, 2022.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K212883ers2 - ergoline Rehabilitation SystemJuly 15, 2022
K112121ERGOSELECT/GEOctober 31, 2012
K053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PApril 27, 2006

FDA data resources