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REMEL

REMEL, INC. · Model R21259 · UDI-DI 00848838023484

LDX
1
510(k) clearances
1
Adverse events
0
Recalls
10
Facilities

Description

PVA-Modified Fixative 500ml Each

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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.