TRANSLITE

FDA Device Registration & Listing · SUGAR LAND, TX, US · Registration 1648557

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
1648557
FEI Number
3000205606
Entity Name
TRANSLITE
City/State/Country
SUGAR LAND, TX, US
Establishment Address
345 Commerce Green Blvd, SUGAR LAND, TX 77478, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
TransLite,LLC (Owner Number: 9023110)
Owner / Operator Contact Address
345 Commerce Green Blvd, Sugar Land, TX 77478, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VEINLITE II VEINLITE VEINLITE220 NEVOSCOPE VEINLITE EMS PRO VEINLITE LED+ VEINLITE NEO VEINLITE LEDX VEINLITE PEDI2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IBJ Light, Microscope Pathology Class 1 864.3600 1995-12-22
KYT Light, Examination, Medical, Battery Powered General Hospital Class 1 880.6350 2005-07-15

Official Correspondent

NIZAR MULLANI

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TransLite,LLC
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 1648557. Last updated year: 2026. Please use registration number 1648557 when referencing this establishment in official correspondence.
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