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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