MRIMed Inc. DBA: Quality Safety Tools

FDA Device Registration & Listing · Petaluma, CA, US · Registration 3009560891

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
3009560891
FEI Number
3009560891
Entity Name
MRIMed Inc. DBA: Quality Safety Tools
City/State/Country
Petaluma, CA, US
Establishment Address
1320 Stub Rd, Petaluma, CA 94954, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Quality Safety Tools DBA: MRIMED (Owner Number: 10040410)
Owner / Operator Contact Address
1320 Stub Rd, Petaluma, CA 94954, 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
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2021-09-07
GDX Scalpel, One-Piece General, Plastic Surgery Class 1 878.4800 2015-05-05
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2021-09-07
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2019-03-18
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2015-05-05
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2015-05-05
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2015-05-05

Official Correspondent

Nader Husary

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Quality Safety Tools DBA: MRIMED
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
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13
K831001 Frontier Products UNICUFF-BLOOD PRESSURE CUFF 1983-07-28
K253089 Shenzhen Best Electronics Co., Ltd. NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722) 2026-02-13
K972301 Rudolf Riester GmbH & Co. KG BIG BEN SQUARE, BIG BEN ROUND 1997-09-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0144-2024 Covidien 1
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009560891. Last updated year: 2026. Please use registration number 3009560891 when referencing this establishment in official correspondence.
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