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FDA 510(k) Applications Submitted by Renovia Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180637
03/12/2018
leva Pelvic Floor Trainer
Renovia Inc.
K192270
08/22/2019
LEva Pelvic Digital Health System
Renovia Inc.
K212495
08/09/2021
Leva Pelvic Health System
Renovia Inc.
K213913
12/15/2021
leva Pelvic Health System
Renovia Inc.
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