Genosis , Ltd.

FERTELL MALE FERTILITY TEST

All identifiers (2)

Aletia (canonical)ALT-001628

FDA 510(k) · US (primary)K041039

Regulatory Registrations

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FDA

ID: K041039

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

This listing was auto-populated from public registry data

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