Orthodynamix, LLC

Orthodynamix, LLC holds 1 FDA 510(k) medical device clearance, cleared in 2010.

Top product codes for Orthodynamix, LLC

GEI — General, Plastic Surgery1 device

Recent clearances by Orthodynamix, LLC

K093086 — ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080Code GEI·2010-02-23

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