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Sign in to claim this brandFerndale Laboratories, Inc.
US
Last updated September 17, 2026
About
Ferndale UK is a trusted dermatology and skincare partner. As a UK customer-focused company, our mission is to supply advanced dermo-cosmetic skincare and specialised skin medicines that enhance skin health, radiance, and overall well-being. Learn more about Ferndale Pharma UK.
From the manufacturer's own website. Source
Information
- Country
- US
- Address
- 780 W 8 Mile Rd, Ferndale, MI, 48220
- Website
- ferndalepharmagroup.com
- —
- —
- [email protected] (from company website)
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1811212
- DUNS Number
- —
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Detachol | 1 | FDA UDI | Class I | Active |
| Detachol | 1 | FDA UDI | Class I | Active |
| Mastisol | 1 | FDA UDI | Class I | Active |
| Detachol | 1 | FDA UDI | Class I | Active |
| Mastisol | 1 | FDA UDI | Class I | Active |
| Detachol | 1 | FDA UDI | Class I | Active |
| Mastisol | 1 | FDA UDI | Class I | Active |
| Detachol | 1 | FDA UDI | Class I | Active |
| Mastisol | 1 | FDA UDI | Class I | Active |
| Detachol | 1 | FDA UDI | Class I | Active |
| Locobase Wound And Skin Emulsion | K060272 | FDA 510(k) | U | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 25, 2025 | Z-1005-2026 | — | open, classified | Butyrate tube cracks during actuation, rendering product unusable. |
| Jul 7, 2010 | Z-0413-2011 | — | terminated | There is a defect on the neck surface of the bottles, causing bottles to leak. Bottle defect may potentially cause contamination of solvent stored in bottles. |