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Kotex

Kimberly Clark Costa Rica Ltda · Model Pad · UDI-DI 07441008154198

HHD

510(k) clearances

138

Adverse events

Recalls

314

Facilities

Description

TOA FEM KOT NOCT TELA C/A 16X8 PR

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.