IndexMethodologyInsightsFor CliniciansRequest Review
Index/Dyansys Corp
ALT-001991K072353Amber Status

Dyansys Corp

PORTABLE ECSCOPE

All identifiers (2)
Aletia (canonical)ALT-001991
FDA 510(k) ยท US (primary)K072353

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K072353
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
Some fields are incomplete or unverified. If you represent Dyansys Corp, you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index