IndexMethodologyInsightsFor CliniciansFor RegulatorsRequest Review
Index/Pearl, Inc.
ALT-006310K243989Green Status

Second Opinion® 3D

Pearl, Inc. · Manufacturer

All identifiers (2)
Aletia (canonical)ALT-006310
FDA 510(k) · US (primary)K243989

Overview

Accountability Tier
Tier 2

Regulatory Registrations

🌐
US
FDA
ID: K243989
510k

Lifecycle Signals

Last Automated Sync
Jun 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
Some fields are incomplete or unverified. If you represent Pearl, Inc., you can verify and update this listing.
Verify this listing →
← Back to Index