FDA Device Establishments · JSON-LD · Markdown
FEI 3003452144 · Manufacture Medical Device · Status: Active
| FEI Number | 3003452144 |
|---|---|
| Owner / Operator | DermLite LLC (#9045109) |
| Address | 21 Argonaut, Unit A, Aliso Viejo, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KYT |
| Regulation § (21 CFR) | 880.6350 |
| Proprietary names | DermLite DL100; DermLite Lumio S (DLUS); DermLite DL4W; DermLite Foto X; DermLite DL200 Hybrid; Syris v900L; DermLite 3 (DL3N); DermLite Lumio (LUM); DermLite DL200 HYG; DermLite HUD2 (HUD2) |
Source: openFDA. Public-domain (CC0).