FDA Device Intelligence
Home › Ahold U.S.A., Inc. › CareOne

CareOne

Ahold U.S.A., Inc. · Model UVH · UDI-DI 00041520044969

JES
10
510(k) clearances
649
Adverse events
0
Recalls
345
Facilities

Description

Floss, Mint, 200YD

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.