Ferndale Laboratories, Inc.
FDA Regulatory Profile
Ferndale Laboratories, Inc. appears in FDA public data with 1 recall, 1 510(k) clearance, 12 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1005-2026, Class II) was initiated on November 25, 2025. Its most recent 510(k) clearance was granted on January 12, 2007.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 12
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1005-2026 | Class II | Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 | November 25, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K060272 | LOCOBASE WOUND AND SKIN EMULSION | January 12, 2007 |