FDA Device Intelligence
Home › LEONE SPA › LEONE SPA

LEONE SPA

LEONE SPA · Model M4800-001 · UDI-DI 08033707068211

DZB Prescription
10
510(k) clearances
17
Adverse events
0
Recalls
27
Facilities

Description

EXORAL FACEBOWS 045 STANDARD LONG

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.