Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3037005063

FEI Number

3037005063

Entity Name

SKINLENS LLC

City/State/Country

St Petersburg, FL, US

Establishment Address

7901 4th St N # 30960, St Petersburg, FL 33702, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SkinLens LLC (Owner Number: 10093019)

Owner / Operator Contact Address

7901 4th St N, #30960, St Petersburg, FL 33702, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SkinLens Skin Lens Skinlens SKIN LENS SKINLENS

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	2025-03-18

Official Correspondent

Connor Stonesifer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SkinLens 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 3037005063. Last updated year: 2026. Please use registration number 3037005063 when referencing this establishment in official correspondence.