INTERFOCUS INC.

FDA Device Registration & Listing · Mountain View, CA, US · Registration 3043515178

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
3043515178
FEI Number
3043515178
Entity Name
INTERFOCUS INC.
City/State/Country
Mountain View, CA, US
Establishment Address
650 CASTRO STREET, STE 120-458, Mountain View, CA 94041, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Interfocus Inc. (Owner Number: 10095183)
Owner / Operator Contact Address
650 CASTRO STREET, STE 120-458, Mountain View, CA 94041, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K252342
PMA Number
N/A

All Registered Proprietary Names

Electric Breast Pump(Model: H03)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2026-02-04

Official Correspondent

Chris Ye

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Interfocus Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190465 Hygeia II Medical Group, Inc. Evolve Breast Pump 2019-10-18
K021739 Limerick, Inc. LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043515178. Last updated year: 2026. Please use registration number 3043515178 when referencing this establishment in official correspondence.
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