ENVIROLITE

FDA Device Registration & Listing · Coldwater, MI, US · Registration 3010033804

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
3010033804
FEI Number
3010033804
Entity Name
ENVIROLITE
City/State/Country
Coldwater, MI, US
Establishment Address
421 Race St, Coldwater, MI 49036, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Envirolite (Owner Number: 10051868)
Owner / Operator Contact Address
421 Race St, Coldwater, MI 49036, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Endoscopy Cleaning Sponge Anchor Pad

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MNL Accessories, Cleaning Brushes, For Endoscope Gastroenterology, Urology Class 1 876.1500 2019-03-15
FWZ Operating Room Accessories Table Tray General, Plastic Surgery Class 1 878.4950 2026-03-05

Official Correspondent

Vatche Tazian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Envirolite
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 3010033804. Last updated year: 2026. Please use registration number 3010033804 when referencing this establishment in official correspondence.
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