FDA Device Intelligence
HomeAEON BIOTHERAPEUTICS CORP. › Aeon CPKit

Aeon CPKit

AEON BIOTHERAPEUTICS CORP. · Model APA-15G · UDI-DI 04719875912016

ORG
0
510(k) clearances
432
Adverse events
0
Recalls
105
Facilities

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.