Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029633864

FEI Number

3029633864

Entity Name

KCL MANUFACTURING, LLC

City/State/Country

Boca Raton, FL, US

Establishment Address

6460 E Rogers Cir, Boca Raton, FL 33487, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

KCL Manufacturing, LLC (Owner Number: 10088922)

Owner / Operator Contact Address

6460 E Rogers Cir, Boca Raton, FL 33487, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CiraPro

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	2025-12-29

Official Correspondent

Kerry Lightcap

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KCL Manufacturing, LLC

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3016214547	RED DOT LED LIGHTING LIMITED	Shenzhen Guangdong, CN
3014296246	PHOTON THERAPY SYSTEMS (PTY) LTD	Pretoria Gauteng, ZA
3033920804	CHONGQING YUYI TECHNOLOGY., CO., LTD.	Chongqing, CN
3015466811	REV-MED INC.	Yongin-si Gyeonggi, KR
3035879449	DONGGUAN JIAYU ELECTRICAL CO.,LTD	Dongguan Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029633864. Last updated year: 2026. Please use registration number 3029633864 when referencing this establishment in official correspondence.