Remex clears universal instruments for its spine navigation system

FDA decision · Remex Medical

20 August 2026

Taiwan-based Remex received clearance for universal navigated instruments that extend its spine navigation system.

Type: FDA decision
Company: Remex Medical
Device: Remex Spine Surgery Navigation – Universal Instruments
Date: 20 August 2026
Jurisdiction: US
Classification: 510(k) K262506 (OLO)
Source: FDA 510(k) database

Official source →Source checked

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