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Biomerics
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
6
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K190259
Vesta RF Cannula
February 7, 2020
K121773
NIMBUS ELECTROSURGICAL RADIOFREQUENCY MULTITINED EXPANDABLE ELECTRODE
September 21, 2012