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Rapport - Vacuum Therapy Device

OWEN MUMFORD USA INCORPORATED · Model SM 2000 · UDI-DI 00384702000019

LKY Prescription
10
510(k) clearances
17
Adverse events
0
Recalls
48
Facilities

Description

A non-sterile, reusable vacuum therapy impotence management system.

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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.