FDA Device Intelligence
HomeBOUND TREE MEDICAL, LLC › Curaplex

Curaplex

BOUND TREE MEDICAL, LLC · Model 670165 · UDI-DI 00817617029535

KSZ
4
510(k) clearances
10,401
Adverse events (6 deaths)
0
Recalls
29
Facilities

Description

Blood Eldon Card Kit (10 Pack)

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.