Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010393950

FEI Number

3010393950

Entity Name

LONG ISLAND TECHNOLOGY GROUP LLC

City/State/Country

Farmingdale, NY, US

Establishment Address

60 Carolyn Boulevard, Farmingdale, NY 11735, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Long Island Technology Group LLC (Owner Number: 10044944)

Owner / Operator Contact Address

60 Carolyn Boulevard, Farmingdale, NY 11735, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Battery-powered medical examination light. Daymark Dover Bristol Hatteras AtoN Fiberoptic Headlight ChromaLUME ; XtremeBeam LIGHT, SURGICAL, FIBEROPTIC

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	2014-08-14
FSW	Light, Surgical, Endoscopic	General, Plastic Surgery	Class 2	878.4580	2015-10-26
FST	Light, Surgical, Fiberoptic	General, Plastic Surgery	Class 2	878.4580	2014-08-14

Official Correspondent

Allan Katz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Long Island Technology Group LLC

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
K901491	Cuda Products Co.	CUDA SURGICAL LIGHT	1990-06-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010393950. Last updated year: 2026. Please use registration number 3010393950 when referencing this establishment in official correspondence.