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Index/Embryotech Laboratories, Inc.
ALT-001343K011679Amber Status

Embryotech Laboratories, Inc.

FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFERTILITY

All identifiers (2)
Aletia (canonical)ALT-001343
FDA 510(k) ยท US (primary)K011679

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K011679
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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