Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043089088

FEI Number

3043089088

Entity Name

BLUE ATLAS LTD

City/State/Country

Hong Kong, CN

Establishment Address

11F, UNIT B, Yam Tze Commercial Building, 23 Thomson Road, Wan Chai, Hong Kong 999077, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Blue Atlas Ltd (Owner Number: 10094541)

Owner / Operator Contact Address

11F, UNIT B, Yam Tze Commercial Building, 23 Thomson Road, Wan Chai, Hong Kong, CN-NOTA 999077, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SURGE COMPACT, SURGE REGENERATION, SURGE OPTIMA, SURGE ExP, REDLIFT, SURGE HEADWAVE, SURGE FOCUS, ARC KNEEVA, LEVELUP RECOVERY+, ARC XBACK, ARC RYNO, ARC RYNO Mi, ARC ATHLETE RECOVERY (LED THERAPY LIGHT)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2025-12-05

Official Correspondent

Richard Mathias

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Blue Atlas Ltd

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 3043089088. Last updated year: 2026. Please use registration number 3043089088 when referencing this establishment in official correspondence.