ResMed West Coast Warehouse

FDA Device Registration & Listing · Moreno Valley, CA, US · Registration 3007009701

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
3007009701
FEI Number
3007009701
Entity Name
ResMed West Coast Warehouse
City/State/Country
Moreno Valley, CA, US
Establishment Address
24960 San Michele Rd, Moreno Valley, CA 92551, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
RESMED CORP. (Owner Number: 9002319)
Owner / Operator Contact Address
9001 Spectrum Center Blvd, --, San Diego, CA 92123, 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
BZD Ventilator, Non-Continuous (Respirator) Anesthesiology Class 2 868.5905 2011-04-20
BZD Ventilator, Non-Continuous (Respirator) Anesthesiology Class 2 868.5905 2011-02-09

Official Correspondent

David Lanfranchi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017684630 ResMed Asia Pte. Ltd. Singapore South West, SG
3011205710 ResMed Corp Lithia Spgs, GA, US
3007573469 RESMED CORP San Diego, CA, US
3038236812 ResMed Malaysia Operations Sdn Bhd Senai Johor, MY
3030970580 RMO Johor Bahru, MY

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K792722 Novametrix Medical Systems, Inc. NOVAMETRIX CPAP NASAL CANNULA 1980-01-24
K082979 Resmed, Ltd. S8 ADVANCE 2009-01-02
K203126 Resmed Pty , Ltd. S10 Kirra 2020-12-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2020 TELEFLEX-MORRISVILLE 2
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
Z-0020-2020 Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan 2
Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
Z-0021-2020 Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan 2
Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold, REF 1002, Rx Only, UDI: 24710810093559
Z-0022-2020 Galemed Corporation 87 Wu-Jia Li-Gong 2nd Road I-Lan Taiwan 2
Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Tube and Oxygen Sensor Port, REF 2691, Rx Only, UDI: 04710810100802

Similar Registrations

Registration Number Establishment Name Location
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3013505405 BMC (Tianjin) Medical Co., Ltd. Wuqing District Tianjin, CN
3033530343 BMC INVESTMENT HOLDING LIMITED Hong Kong, HK
3017684630 ResMed Asia Pte. Ltd. Singapore South West, SG
3042507287 3B MEDICAL INC W Jefferson, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007009701. Last updated year: 2026. Please use registration number 3007009701 when referencing this establishment in official correspondence.
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