Trividia Health, Inc.

FDA Device Registration & Listing · Fort Lauderdale, FL, US · Registration 1000113657

Public Record Device Listing Expiry Year: 2026 AvaSpecs displays structured public-record fields for easier browsing and citation.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1000113657
FEI Number
1000113657
Entity Name
Trividia Health, Inc.
City/State/Country
Fort Lauderdale, FL, US
Establishment Address
2400 NW 55TH CT, Fort Lauderdale, FL 33309, US
Establishment Type(s)
Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
TRIVIDIA HEALTH, INC. (Owner Number: 9000560)
Owner / Operator Contact Address
2400 N.W. 55TH CT., --, Ft Lauderdale, FL 33309, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

TRUE METRIX AIR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NBW System, Test, Blood Glucose, Over The Counter Clinical Chemistry Class 2 862.1345 2015-05-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000113657. Last updated year: 2026. Please use registration number 1000113657 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
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