FDA Device Intelligence
Home › NORDENT MANUFACTURING INC › Nordent Manufacturing, Inc.

Nordent Manufacturing, Inc.

NORDENT MANUFACTURING INC · Model RCAW2A-BRLAD3B · UDI-DI 00840018667464

EIY Prescription
5
510(k) clearances
18
Adverse events
0
Recalls
189
Facilities

Description

Composite Placement, DE, Ward Paddle - Ladmore plugger

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.