FDA Device Intelligence
Home › Zeltiq Aesthetics, Inc. › SP3 Dermalinfusion

SP3 Dermalinfusion

Zeltiq Aesthetics, Inc. · Model A0142 · UDI-DI 00816417021848

GFE Prescription
2
510(k) clearances
47
Adverse events
0
Recalls
157
Facilities

Description

SP3 Dermalinfusion, 110V

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.