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Sign in to claim this brandDermLite LLC
United States·US-MF-000005170
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 21 Argonaut, Aliso Viejo CA, United States
- Website
- dermlite.com/
- —
- —
- [email protected]
- Phone
- +1 949-481-6384
- PRRC Contact
- Paula Wojtaszek
- EUDAMED SRN
- US-MF-000005170
- FDA FEI Number
- 3003452144
- DUNS Number
- 104621896
Catalogue (182)
Page 1 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FOTO Cable (Head to PowerPack) | FOTO-CABLE | FDA UDI | Class I | Active |
| Lumio | LUM | FDA UDI | Class I | Active |
| DermLite DL5 Charging Base | DL5-CB | FDA UDI | Class I | Active |
| DermLite Foto X Plus | DLFX-Plus | FDA UDI | Class I | Active |
| DermLite Carbon | DLC | FDA UDI | Class I | Active |
| DermLite Universal Smartphone Adapter | DLUA | FDA UDI | Class I | Active |
| DermLite Cam | DLcam | FDA UDI | Class I | Active |
| MagnetiConnect® for Nikon 1 Series | DLMC-N1 | FDA UDI | Class I | Active |
| INACTIVE - Skinlite | SKL1 | FDA UDI | Class I | Active |
| INACTIVE - Nailio | NL1 | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 7/8 Plus | DLCKi7+ | FDA UDI | Class I | Active |
| DL4 Magnetic Eyepiece | DL4EP | FDA UDI | Class I | Active |
| USB-C to USB-C cable, 2m | USB-CC2 | FDA UDI | Class I | Active |
| DermLite GL Battery | GLB | FDA UDI | Class I | Active |
| INACTIVE - Skinlite II | SKL2 | FDA UDI | Class I | Active |
| DermLite Immersion Fluid | DLFO | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S5 | DLCKG5 | FDA UDI | Class I | Active |
| FOTO PowerPack | FOTO-Powerpack | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S9 | DLCKG9 | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 5C | DLCKi5C | FDA UDI | Class I | Active |
| DL Connection Kit for iPad 5/6 | DLCKiP5 | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Mini | DLCKiPM | FDA UDI | Class I | Active |
| MagnetiConnect Clamp | MCC | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 7/8 | DLCKi7 | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S7 | DLCKG7 | FDA UDI | Class I | Active |
| MagnetiConnect Adapter - 58 mm | DLMC-58 | FDA UDI | Class I | Active |
| MagnetiConnect Adapter - 49 mm | DLMC-49 | FDA UDI | Class I | Active |
| DL Connection Kit for iPad 3/4 | DLCKiP | FDA UDI | Class I | Active |
| MagnetiConnect Kit - Smartphone/Tablet Adapter | MCK | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Air2 | DLCKiPA2 | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S6 | DLCKG6 | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 6 Plus | DLCKi6+ | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 6 | DLCKi6 | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S8 | DLCKG8 | FDA UDI | Class I | Active |
| DL200/Lumio S Drawstring Pouch | DSP | FDA UDI | Class I | Active |
| DermLite DL5 | DL5 | FDA UDI | Class I | Active |
| MagnetiConnect for Nikon 1 AW1 | DLMC-N1 | FDA UDI | Class I | Active |
| DL Connection Kit for iPod Touch 6 | DLCKiPT | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S4 | DLCKG4 | FDA UDI | Class I | Active |
| DermLite DL4 | DL4 | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Mini 4 | DLCKiPM4 | FDA UDI | Class I | Active |
| DL Connection Kit for Galaxy S8+ | DLCKG8+ | FDA UDI | Class I | Active |
| DermLite DL1 | DL1 | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone SE/5 | DLCKi5 | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Pro 9.7 | DLCKiPPro | FDA UDI | Class I | Active |
| DL Connection Kit for iPhone 4 | DLCKi4 | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Pro 10.5 | DLCKiPP10.5 | FDA UDI | Class I | Active |
| PowerPack Charger | FOTO-CHARGER | FDA UDI | Class I | Active |
| DL Connection Kit for iPad Air | DLCKIPA | FDA UDI | Class I | Active |
| DL200 Silicone Sleeve, clear | DL200CS | FDA UDI | Class I | Active |
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FDA Recalls (1)
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 |
|---|---|---|---|---|
| Mar 20, 2023 | Z-1506-2023 | — | open, classified | Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling. |