HUELIGHT USA

FDA Device Registration & Listing · Rock Hill, NY, US · Registration 3030648305

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
3030648305
FEI Number
3030648305
Entity Name
HUELIGHT USA
City/State/Country
Rock Hill, NY, US
Establishment Address
146 Rock Hill Drive, Rock Hill, NY 12775, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Huelight USA (Owner Number: 10090075)
Owner / Operator Contact Address
146 Rock Hill Drive, PO Box 960, Rock Hill, NY 12775, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cannula Breast PBM Irradiator Whole Body PBM PBM Full Body Panel w/ Stand Abdomen PBM Irradiator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2024-02-12
CAT Cannula, Nasal, Oxygen Anesthesiology Class 1 868.5340 2024-02-12
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-02-12

Official Correspondent

Darren Schwartz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821133 Durham Electric Co. ELECTRICAL VIBRATING DEVICE 1982-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030648305. Last updated year: 2026. Please use registration number 3030648305 when referencing this establishment in official correspondence.
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