FDA Device Intelligence
Home › MEDLINE INDUSTRIES, INC. › Medline

Medline

MEDLINE INDUSTRIES, INC. · Model MDS6303001 · UDI-DI 10888277632110

HDX Prescription
9
510(k) clearances
4
Adverse events
1
Recalls
19
Facilities

Description

DILATOR, SILICONE, VAGINAL SET, LARGE

Recalls

DateFirmReason
2015-06-19CooperSurgical, Inc.Incorrect expiration date on outer carton kit label

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.