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

Bausch + Lomb

Bausch & Lomb Incorporated · Model SP7-62478 · UDI-DI 00757770636631

HND Prescription
6
510(k) clearances
90
Adverse events
0
Recalls
161
Facilities

Description

E4937 M MANIPULATOR TITANIUM

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.