FDA Device Intelligence
Home › Kimberly Clark Costa Rica Ltda › Kotex

Kotex

Kimberly Clark Costa Rica Ltda · Model Pad · UDI-DI 07441008164326

HHD
10
510(k) clearances
138
Adverse events
0
Recalls
317
Facilities

Description

TOA FEM KOT ESENC NOR TELA S/A 24X10 PR

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.