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Breathewave

BREATHEWAVE TECHNOLOGIES INC. · Model Large · UDI-DI 00860014485268

LWF

510(k) clearances

228

Adverse events (2 deaths)

Recalls

121

Facilities

Description

Contoured Nasal Dilator

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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.