# DermLite LLC

FEI: 3003452144
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: DermLite LLC (#9045109)

Address: 21 Argonaut, Unit A, Aliso Viejo, CA, US



## Products

Total registered: 1
Top product codes: KYT
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003452144%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003452144