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

Bausch + Lomb

Bausch & Lomb Incorporated · Model E0828 A · UDI-DI 00757770408993

HNA Prescription
2
510(k) clearances
1
Adverse events
0
Recalls
91
Facilities

Description

NDL TP F/E828 SPUD NDL & GOUGE

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.