Pherdal Fertility Science, Inc.
Pherdal Fertility Science, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent FDA inspection ended on Jul 9, 2026 (No Action Indicated (NAI)). Its most recent 510(k) clearance was granted on Dec 14, 2023.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jul 9, 2026 | Dixon, IL | Devices | No Action Indicated (NAI) | 3020796587 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K231645 | PherDal® At-Home Insemination Kit | Dec 14, 2023 |