SEQUITUR HEALTH CORP.

FDA Device Registration & Listing · Phoenix, AZ, US · Registration 3023591031

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
3023591031
FEI Number
3023591031
Entity Name
SEQUITUR HEALTH CORP.
City/State/Country
Phoenix, AZ, US
Establishment Address
6161 E Mayo Blvd, STE 221D, Phoenix, AZ 85054, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Sequitur Health Corp. (Owner Number: 10094473)
Owner / Operator Contact Address
6161 E Mayo Blvd, STE 221D, Phoenix, AZ 85054, US
Initial Importer Flag
Y
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
JRC Micro Pipette Clinical Chemistry Class 1 862.2050 2025-12-02

Official Correspondent

Marylaura Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sequitur Health Corp.
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 3023591031. Last updated year: 2026. Please use registration number 3023591031 when referencing this establishment in official correspondence.
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