IXLAYER

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3031090645

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
3031090645
FEI Number
3031090645
Entity Name
IXLAYER
City/State/Country
San Francisco, CA, US
Establishment Address
447 Sutter Street, Suite 405, PMB 53, San Francisco, CA 94108, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ixlayer (Owner Number: 10090689)
Owner / Operator Contact Address
447 Sutter Street, Suite 405, PMB 53, San Francisco, CA 94108, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Celiac Assessment Cholesterol Lyme Disease Type 1 Diabetes Autoantibody Screening Vitamin D Eosinophilic Asthma Screening Heart Health & Diabetes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PQD Blood Specimen Collection Convenience Kit (Excludes Hiv) Clinical Chemistry Class 2 862.1675 2024-04-29
OIB Blood And Urine Collection Kit (Excludes Hiv Testing) Pathology Class 1 864.3250 2024-10-24

Official Correspondent

Shivanie Plaza

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ixlayer
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 3031090645. Last updated year: 2026. Please use registration number 3031090645 when referencing this establishment in official correspondence.
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