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Femasys, Inc.

9 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
FemVue® Controlled Saline-Air Device (FSA-300) (K253403)Femasys, Inc.2025-12-15
FemVue MINI Saline-Air Device (K242002)Femasys, Inc.2024-11-22
FemChec Controlled Saline-Air Device (FCD-250) (K241693)Femasys, Inc.2024-09-06
FemaSeed Intratubal Insemination (K231730)Femasys, Inc.2023-09-22
FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009 (K122658)Femasys, Inc.2012-12-20
FEMCHEC PRESSURE MANAGEMET DEVICE (K110993)Femasys, Inc.2011-10-12
FEMVUE SALINE-AIR DEVICE (K110288)Femasys, Inc.2011-04-28
FEMVUE CORNUAL BALLOON CATHETER (K100662)Femasys, Inc.2010-04-07
FEMVUE(TM) CATHETER SYSTEM (K083690)Femasys, Inc.2009-06-23

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Every clearance here is in the API, with alerts when new ones post.