FDA Device Intelligence
Home › LEONE SPA › LEONE SPA

LEONE SPA

LEONE SPA · Model M3051-04 · UDI-DI 08033707068129

EHP Prescription
8
510(k) clearances
0
Adverse events
0
Recalls
24
Facilities

Description

LIP BUMPER 045 WITH LOOPS/STOP n. 4

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.