FDA Device Intelligence
Home › PMT CORPORATION › ALLURA®

ALLURA®

PMT CORPORATION · Model 3321-13-T · UDI-DI 00650551003236

KXP Prescription
1
510(k) clearances
1
Adverse events
0
Recalls
7
Facilities

Description

VAGINAL STENT, CYLINDRICAL, 4X13CM, PROJECTION 4CM, FILL 157CC, 2 SUTURE TABS

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.