VIVAPRODUCTS, INC.

FDA Device Registration & Listing · Littleton, MA, US · Registration 1224838

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
1224838
FEI Number
1000513605
Entity Name
VIVAPRODUCTS, INC.
City/State/Country
Littleton, MA, US
Establishment Address
521 GREAT RD, Littleton, MA 01460, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Vivaproducts (Owner Number: 10050765)
Owner / Operator Contact Address
521 Great Road, Littleton, MA 01460, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vivafree 2; Vivafree 500; Vivaspin 20; Vivaspin 15; Vivaspin 6; Vivaspin 4 BJP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JJH Clinical Sample Concentrator Clinical Chemistry Class 1 862.2310 2015-12-23

Official Correspondent

Robert Tutunjian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vivaproducts
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 1224838. Last updated year: 2026. Please use registration number 1224838 when referencing this establishment in official correspondence.
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