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RNARetain

ASURAGEN, INC. · Model 84001 · UDI-DI 00863840000285

OZF
1
510(k) clearances
0
Adverse events
0
Recalls
1
Facilities

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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.