FDA Device Intelligence
Home › MEIJER, INC. › Meijer

Meijer

MEIJER, INC. · Model 6C9 · UDI-DI 00719283862181

JES
10
510(k) clearances
651
Adverse events
0
Recalls
348
Facilities

Description

Flosser, Hi-Tech, Curvy, Mint

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.