TIDEPOOL PROJECT

FDA Device Registration & Listing · Palo Alto, CA, US · Registration 3012128418

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
3012128418
FEI Number
3012128418
Entity Name
TIDEPOOL PROJECT
City/State/Country
Palo Alto, CA, US
Establishment Address
3340 Hillview Ave., Palo Alto, CA 94304, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Tidepool Project (Owner Number: 10050969)
Owner / Operator Contact Address
555 Bryant St., #429, Palo Alto, CA 94301, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tidepool Data Management Platform Tidepool Plus Tidepool+ Tidepool Data Platform Tidepool Mobile Tidepool Web Tidepool Cloud Platform Tidepool Uploader

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PHV Continuous Glucose Monitor Retrospective Data Analysis Software Clinical Chemistry Class 1 862.2120 2016-01-21
OUG Medical Device Data System General Hospital Class 1 880.6310 2016-01-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tidepool Project
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 3012128418. Last updated year: 2026. Please use registration number 3012128418 when referencing this establishment in official correspondence.
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