FDA Device Intelligence
HomeThe Myerson Company Limited › Kenson

Kenson

The Myerson Company Limited · Model T18C3L0X34 · UDI-DI 00842326121997

ELM Prescription
1
510(k) clearances
56
Adverse events
0
Recalls
102
Facilities

Description

30° Posterior shade C3, mould X34, L

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.