Refine USA, LLC

Refine USA, LLC holds 2 FDA 510(k) medical device clearances, first cleared 2012, most recent 2020.

Top product codes for Refine USA, LLC

ONQ — General, Plastic Surgery1 device
QAI — General, Plastic Surgery1 device

Recent clearances by Refine USA, LLC

K192138 — Rejuvapen NXTCode QAI·2020-04-09
K112334 — VEIN-GOGH INSTRUMENTCode ONQ·2012-05-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.