FDA Device Intelligence
Home › Bausch & Lomb Incorporated › Bausch + Lomb

Bausch + Lomb

Bausch & Lomb Incorporated · Model N5941 2 · UDI-DI 00757770414130

MSR Prescription
5
510(k) clearances
10
Adverse events
0
Recalls
2
Facilities

Description

SILICONE TUBE .020"x.037"x10FT

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.