SIPHOX, INC.

FDA Device Registration & Listing · Burlington, MA, US · Registration 3018308579

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
3018308579
FEI Number
3018308579
Entity Name
SIPHOX, INC.
City/State/Country
Burlington, MA, US
Establishment Address
111 Terrace Hall Ave, Burlington, MA 01803, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
SiPhox, Inc. (Owner Number: 10094290)
Owner / Operator Contact Address
111 Terrace Hall Ave, Burlington, MA 01803, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SiPhox collection kit v1 SiPhox collection kit v1.2 SiPhox collection kit v1.1

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 2026-01-15

Official Correspondent

Cameron Habib

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SiPhox, Inc.
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 3018308579. Last updated year: 2026. Please use registration number 3018308579 when referencing this establishment in official correspondence.
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