FDA Device Intelligence
HomeTwin Med, LLC › ProCure

ProCure

Twin Med, LLC · Model PCCTAS6 · UDI-DI 10840330701485

KXF
10
510(k) clearances
552
Adverse events (6 deaths)
2
Recalls
369
Facilities

Description

ProCure Applicators Cotton-Tip 6" Sterile 2ea/pk 100pk/bx 10bx/cs

Recalls

DateFirmReason
2023-02-03Avanos Medical, Inc.Incorrect expiration date.
2013-03-26Owens & Minor Distribution, Inc.Owens & Minor Distribution, Inc. is conducting a market withdrawal of MediChoice Applicator OB-GYN 8 inch product that does not meet our quality standards because the rayon may loo

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.