Anx Robotica Corporation

Anx Robotica Corporation holds 3 FDA 510(k) medical device clearances, first cleared 2023, most recent 2025.

Top product codes for Anx Robotica Corporation

Recent clearances by Anx Robotica Corporation

K250493 — MotiliCap GI Monitoring SystemCode NYV·2025-05-21
K233229 — NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam TetherCode NEZ·2024-01-05
K231960 — NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam TetherCode QKZ·2023-10-03

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