REVANCE THERAPEUTICS, INC.

FDA Device Registration & Listing · Newark, CA, US · Registration 3007772056

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007772056
FEI Number
3007772056
Entity Name
REVANCE THERAPEUTICS, INC.
City/State/Country
Newark, CA, US
Establishment Address
7555 Gateway Blvd, Newark, CA 94560, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Revance Therapeutics, Inc. (Owner Number: 10062439)
Owner / Operator Contact Address
1222 Demonbreun Street, Suite 2000, Nashville, TN 37203, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P170002

All Registered Proprietary Names

RHA® 2; RHA® 2 Mepi; RHA® 3; RHA® 3 Mepi; RHA® 4; RHA® 4 Mepi; RHA® Dynamic Volume; RHA® Redensity; RHA® Redensity Mepi

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2024-08-30

Official Correspondent

Marie Fogartie

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Revance Therapeutics, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007772056. Last updated year: 2026. Please use registration number 3007772056 when referencing this establishment in official correspondence.
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