The O R Company Pty, Ltd.

The O R Company Pty, Ltd. holds 2 FDA 510(k) medical device clearances, cleared in 2022.

Top product codes for The O R Company Pty, Ltd.

LKF — Obstetrics/Gynecology2 devices

Recent clearances by The O R Company Pty, Ltd.

K220202 — Uterine ElevatOR PRO with OccludOR BalloonCode LKF·2022-03-31
K212505 — DUMI ManipulatORCode LKF·2022-01-10

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