Femasys, Inc.
Femasys, Inc. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2025.
Top product codes for Femasys, Inc.
Recent clearances by Femasys, Inc.
- K253403 — FemVue® Controlled Saline-Air Device (FSA-300)
- K242002 — FemVue MINI Saline-Air Device
- K241693 — FemChec Controlled Saline-Air Device (FCD-250)
- K231730 — FemaSeed Intratubal Insemination
- K122658 — FEMCERV ENDOCERVICAL SAMPLER MODEL 3 SIZES: REF FCV-013, REF FCV-011, REF FCV-009
- K110993 — FEMCHEC PRESSURE MANAGEMET DEVICE
- K110288 — FEMVUE SALINE-AIR DEVICE
- K100662 — FEMVUE CORNUAL BALLOON CATHETER
- K083690 — FEMVUE(TM) CATHETER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.