Home › PRESTIGE AMERITECH, LTD. › PremierPro

PremierPro

PRESTIGE AMERITECH, LTD. · Model 3474 · UDI-DI 00811220032876

OMD Prescription

510(k) clearances

2,156

Adverse events (2 deaths)

Recalls

Facilities

Description

EXOFINFUSION® Skin Closure System, 30cm

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 key Read 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.