ALT-001008K063694Amber Status
Bausch & Lomb, Inc.
AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28
All identifiers (2)
Aletia (canonical)
ALT-001008FDA 510(k) · US (primary)
K063694Regulatory Registrations
🌐
US
FDA
ID: K063694
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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