ALT-001053K223347Amber Status
Ultrasight, Inc.
UltraSight AI Guidance
All identifiers (2)
Aletia (canonical)
ALT-001053FDA 510(k) · US (primary)
K223347Overview
Accountability Tier
Tier 2
Regulatory Registrations
🌐
US
FDA
ID: K223347
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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