FDA Device Intelligence
HomeMEDLINE INDUSTRIES, INC. › Medline

Medline

MEDLINE INDUSTRIES, INC. · Model NON27LV30XL · UDI-DI 20197344074454

FXP
10
510(k) clearances
124
Adverse events
0
Recalls
286
Facilities

Description

COVER,BOOT,LV3,FOAM,NON-SKID,XL

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.