FDA Device Intelligence
Home › Smith & Nephew, Inc. › EMPERION

EMPERION

Smith & Nephew, Inc. · Model 71361792 · UDI-DI 03596010591036

JDG Prescription
1
510(k) clearances
6,715
Adverse events (11 deaths)
0
Recalls
58
Facilities

Description

EMP 19 LG CONE 2 SPOUT TRIAL SLEEVE

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.