Home › Beaver-Visitec International, Inc. › Visitec®

Visitec®

Beaver-Visitec International, Inc. · Model 585189 · UDI-DI 30886158102183

HND

510(k) clearances

Adverse events

Recalls

163

Facilities

Description

SPATULA EXCIMER (5/SP)

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.