FDA Device Intelligence
HomePREMIER DENTAL PRODUCTS COMPANY › Traxodent

Traxodent

PREMIER DENTAL PRODUCTS COMPANY · Model 9007094 · UDI-DI 00348783000306

MVL Prescription
1
510(k) clearances
25
Adverse events
1
Recalls
43
Facilities

Description

Traxodent Unit Dose (24)

Recalls

DateFirmReason
2026-05-27Inter-Med LlcSome units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions,

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.