FDA Device Intelligence
Home › NORDENT MANUFACTURING INC › NORDENT MANUFACTURING INC

NORDENT MANUFACTURING INC

NORDENT MANUFACTURING INC · Model CEPFIW2 · UDI-DI 00840018637726

EKD
2
510(k) clearances
26
Adverse events
0
Recalls
73
Facilities

Description

COMPOSITE DE PFIW2 CE HANDLE

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.