SIREN

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3015542388

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
3015542388
FEI Number
3015542388
Entity Name
SIREN
City/State/Country
San Francisco, CA, US
Establishment Address
1256 Folsom St, San Francisco, CA 94103, US
Establishment Type(s)
Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Siren (Owner Number: 10060280)
Owner / Operator Contact Address
1256 Folsom Street, Unit 513, San Francisco, CA 94103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Siren Socks

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OIZ Foot Examination Tool For Inflammatory Changes Physical Medicine Class 1 890.5050 2019-04-19

Official Correspondent

Henk Jan Scholten

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Siren
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 3015542388. Last updated year: 2026. Please use registration number 3015542388 when referencing this establishment in official correspondence.
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