VINELAND SYRUP INC.

FDA Device Registration & Listing · VINELAND, NJ, US · Registration 2226984

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
2226984
FEI Number
2226984
Entity Name
VINELAND SYRUP INC.
City/State/Country
VINELAND, NJ, US
Establishment Address
723 S.E. BLVD., VINELAND, NJ 08360, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VINELAND SYRUP INC. (Owner Number: 9058089)
Owner / Operator Contact Address
723 S.E. BLVD., --, Vineland, NJ 08360, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K120247
PMA Number
N/A

All Registered Proprietary Names

EasyDex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRV Drink, Glucose Tolerance Clinical Chemistry Class 2 862.1345 2012-06-25

Official Correspondent

MEILECH KORNBLUH

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VINELAND SYRUP INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2226984. Last updated year: 2026. Please use registration number 2226984 when referencing this establishment in official correspondence.
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