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/ Ingen Orthopedics, LLC
Ingen Orthopedics, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
5
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K131277
SEVIIN FRACTURE SHOULDER
August 28, 2013
K130635
SEVIIN SURFACE REPLACEMENT SHOULDER
August 26, 2013
K120374
SEVIIN REVERSE SHOULDER
July 9, 2012