Pherdal Fertility Science, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pherdal Fertility Science, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PherDal® At-Home Insemination Kit
1
Total
1
Cleared
0
Denied
Pherdal Fertility Science, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dixon, US.
Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Pherdal Fertility Science, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iuvo Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pherdal Fertility Science, Inc.
1 devices