FDA Device Intelligence
Home › The Myerson Company Limited › Kenson

Kenson

The Myerson Company Limited · Model T1AC1L0029 · UDI-DI 00842326123793

ELM Prescription
1
510(k) clearances
56
Adverse events
0
Recalls
101
Facilities

Description

Block Posterior shade C1, mould 29, 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.