Data / Medical devices / United States / Revance Therapeutics, Inc.
Revance Therapeutics, Inc.: FDA-registered device maker in Newark, CA, United States, 1 PMA approval
Revance Therapeutics, Inc. is registered with the FDA (registration 3007772056) in Newark, CA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated October 19, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007772056
- Address
- 7555 Gateway Blvd, Newark, CA, United States, 94560
- Owner or operator
- Revance Therapeutics, Inc. (10062439)
- Roles
- Complaint file establishment
- First device listed
- August 30, 2024
- Registered through
- 2027
- Brand names listed
- RHA Redensity® Eye, RHA® 2; RHA® 2 Mepi; RHA® 3; RHA® 3 Mepi; RHA® 4; RHA® 4 Mepi; RHA® Dynamic Volume; RHA® Redensity; RHA® Redensity Mepi
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Implant, Dermal, For Aesthetic Use | LMH | 3 | Complaint file establishment | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| October 19, 2017 | P170002 | RHA 2, RHA 3, RHA 4 | LMH | 55 | August 31, 2026 | accessdata.fda.gov |
Compare with other makers
Updated August 31, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.