Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

leva Pelvic Health System

K-Number: K213913 · 2022-06-30

ApplicantRenovia, Inc.
Decision Date2022-06-30
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

leva Pelvic Health System is the device name listed in this FDA 510(k) record. The listed applicant is Renovia, Inc.. It received FDA 510(k) clearance on 2022-06-30 under 510(k) number K213913. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the leva Pelvic Health System?

leva Pelvic Health System is a medical device that received FDA 510(k) clearance on 2022-06-30. The listed applicant is Renovia, Inc.. The 510(k) number is K213913.

When did leva Pelvic Health System receive FDA 510(k) clearance?

leva Pelvic Health System received FDA 510(k) clearance on 2022-06-30, under 510(k) number K213913.

Who is the listed applicant for leva Pelvic Health System?

The FDA 510(k) record lists Renovia, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for leva Pelvic Health System?

The FDA product code for leva Pelvic Health System is HIR.

Other records listing Renovia, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HIR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.