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Renovia, Inc.

FDA Regulatory Profile

Renovia, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 30, 2022.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213913leva Pelvic Health SystemJune 30, 2022
K212495Leva Pelvic Health SystemSeptember 8, 2021
K192270LEva Pelvic Digital Health SystemNovember 22, 2019
K180637leva Pelvic Floor TrainerApril 4, 2018

FDA data resources