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Bausch + Lomb

Bausch & Lomb Incorporated · Model N6065 2 · UDI-DI 00757770420322

KBH Prescription
1
510(k) clearances
1
Adverse events
0
Recalls
38
Facilities

Description

BLD F/N6050,055,060 & 070 MED

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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.