Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003452144

FEI Number

3003452144

Entity Name

DermLite LLC

City/State/Country

Aliso Viejo, CA, US

Establishment Address

21 Argonaut, Unit A, Aliso Viejo, CA 92656, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DermLite LLC (Owner Number: 9045109)

Owner / Operator Contact Address

21 Argonaut, Unit A, Aliso Viejo, CA 92656, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DermLite HUD2 (HUD2) DermLite Lumio S (DLUS) DermLite Lumio UV (LUM UV) DermLite DL4 (DL4) DermLite DL1 Basic (DL1B) DermLite Handyscope Syris v900L DermLite DL4W DermLite DL200 HYG DermLite Carbon (DermLite DLC) DermLite DL100 DermLite 1 (DL1) DermLite GL DermLite DL5P (DL5 Plus) DermLite DL5 (DL5) DermLite Lumio (LUM) DermLite DL200 Hybrid DermLite Foto II Pro (Foto II Pro) DermLite Foto X DermLite DL200 HR DermLite 3 (DL3N) DermLite Lumio 2 (DLU2)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2001-03-14

Official Correspondent

Paula Wojtaszek

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DermLite LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003452144. Last updated year: 2026. Please use registration number 3003452144 when referencing this establishment in official correspondence.