FDA Device Intelligence
Home › Cynosure, LLC › SculpSure laser assembly

SculpSure laser assembly

Cynosure, LLC · Model 100-7026-010 · UDI-DI 00841494100032

PKT Prescription
10
510(k) clearances
72
Adverse events
0
Recalls
16
Facilities

Description

SculpSure laser assembly

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.