NUVANCE* FACIAL REJUVENATION SYSTEM— 510(k) K052953

Name: FDA 510(k) clearance K052953
Creator: U.S. Food and Drug Administration
Published: 2006-03-06

Substantially Equivalent

ETHICON, Inc.

FDA 510(k) clearance K052953 for NUVANCE* FACIAL REJUVENATION SYSTEM, Substantially Equivalent on 2006-03-06. Applicant: ETHICON, Inc.. Device class: 2.

Clearance details

Applicant: ETHICON, Inc.
Product code: Code MXW
Device class: Class 2
Regulation: 21 CFR 878.5010
Advisory panel: General, Plastic Surgery
Date received: 2005-10-20
Decision date: 2006-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sommerville, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MXW

view all

K060465 — PREMIO2007-01-17

More clearances from ETHICON, Inc.

view all

K253394 — Coated VICRYL (Polyglactin 910) Plus Antibacterial Suture2026-06-25
K252047 — STRATAFIX Symmetric PDS Plus Knotless Tissue Control Devices2026-05-18
K253572 — STRATAFIX Spiral PRONOVA Unidirectional Knotless Tissue Control Device STRATAFIX Spiral PRONOVA Bidirectional Knotless Tissue Control Device2026-03-27
K253852 — MONOCRYL Plus Antibacterial Poliglecaprone 25 (Monofilament), Sterile Synthetic Absorbable Surgical Suture2026-02-06
K252743 — STRATAFIX Spiral PDS Plus Knotless Tissue Control Device; STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control Device2025-12-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.