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U By Kotex

KIMBERLY-CLARK GLOBAL SALES, INC. · Model Pad · UDI-DI 00036000549331

HHD
10
510(k) clearances
138
Adverse events
0
Recalls
313
Facilities

Description

U BY KOTEX SUPRPREM ULTTHN EXTRA HEAVY OVRNTWNG PAD 22

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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.