FDA Device Intelligence
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Bausch + Lomb

Bausch & Lomb Incorporated · Model N0610 L · UDI-DI 00757770429233

JZF Prescription
5
510(k) clearances
41
Adverse events
0
Recalls
145
Facilities

Description

SUCT TB EAR HOUS-BARON 5FR LNG

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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.