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Norlake

NOR-LAKE, INCORPORATED · Model NSBF211WWW/0 · UDI-DI 00851714007010

KSE
4
510(k) clearances
383
Adverse events (3 deaths)
0
Recalls
39
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.