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/ Renovia, Inc.
Renovia, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K213913
leva Pelvic Health System
June 30, 2022
K212495
Leva Pelvic Health System
September 8, 2021
K192270
LEva Pelvic Digital Health System
November 22, 2019
K180637
leva Pelvic Floor Trainer
April 4, 2018