FDA Device Intelligence
Home › Dynarex Corporation › Saliva Ejectors

Saliva Ejectors

Dynarex Corporation · Model 2219 · UDI-DI 00616784221915

DYN
10
510(k) clearances
100
Adverse events (1 deaths)
0
Recalls
151
Facilities

Description

Saliva Ejectors Blue Tip/Clear Body

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.