ECOTEC MANUFACTURING

FDA Device Registration & Listing · Okeechobee, FL, US · Registration 3004825240

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
3004825240
FEI Number
3004825240
Entity Name
ECOTEC MANUFACTURING
City/State/Country
Okeechobee, FL, US
Establishment Address
312 SW 7th Ave, Okeechobee, FL 34974, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ecotec Manufacturing (Owner Number: 10053128)
Owner / Operator Contact Address
312 SW 7th Ave, Okeechobee, FL 34974, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IFI Sprays, Synthetic, Smear Pathology Class 1 864.4010 2016-11-02

Official Correspondent

Michael Fishman Fishman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ecotec Manufacturing
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 3004825240. Last updated year: 2026. Please use registration number 3004825240 when referencing this establishment in official correspondence.
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