NEOLIGHT, LLC

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3014128880

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014128880
FEI Number
3014128880
Entity Name
NEOLIGHT, LLC
City/State/Country
Scottsdale, AZ, US
Establishment Address
1475 N Scottsdale Rd Ste 110, Scottsdale, AZ 85257, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
NeoLight, LLC (Owner Number: 10056250)
Owner / Operator Contact Address
1475 N. Scottsdale Rd, Ste110, Scottsdale, AZ 85257, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K170585
PMA Number
N/A

All Registered Proprietary Names

PAL Pacifier Activated Lullaby Neolight Bassinet Basket Skylife Phototherapy System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2022-09-29
NZG Bassinet, Hospital General Hospital Class 2 880.5145 2024-11-26
LBI Unit, Neonatal Phototherapy General Hospital Class 2 880.5700 2017-11-20

Official Correspondent

Erik Dawson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeoLight, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012096560 Phoenix Technology Group LLC Pleasanton, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014128880. Last updated year: 2026. Please use registration number 3014128880 when referencing this establishment in official correspondence.
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