FDA Device Intelligence
HomeDUCKWORTH AND KENT LIMITED › Duckworth & Kent

Duckworth & Kent

DUCKWORTH AND KENT LIMITED · Model 6-181 · UDI-DI 05055313809166

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

Description

Lacrimal Dilator

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.