MED ONE EQUIPMENT SERVICES, LLC

FDA Device Registration & Listing · Sandy, UT, US · Registration 3013652261

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
3013652261
FEI Number
3013652261
Entity Name
MED ONE EQUIPMENT SERVICES, LLC
City/State/Country
Sandy, UT, US
Establishment Address
10712 S 1300 E, Sandy, UT 84094, US
Establishment Type(s)
Sterilize Medical Device for Another Party (Contract Sterilizer),Repack or Relabel Medical Device
Owner / Operator
Med One Equipment Services (Owner Number: 10054899)
Owner / Operator Contact Address
10712 S 1300 E, Sandy, UT 84094, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CareFusion Carefusion CareFusion CareFusion CareFusion Hospira Sigma Medex CareFusion CareFusion

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRN Pump, Infusion General Hospital Class 2 880.5725 2017-05-10
FRN Pump, Infusion General Hospital Class 2 880.5725 2022-02-10
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase Anesthesiology Class 2 868.1400 2017-05-10
FRN Pump, Infusion General Hospital Class 2 880.5725 2017-05-10
FRN Pump, Infusion General Hospital Class 2 880.5725 2017-05-10
FRN Pump, Infusion General Hospital Class 2 880.5725 2018-06-26
FRN Pump, Infusion General Hospital Class 2 880.5725 2018-06-26
FRN Pump, Infusion General Hospital Class 2 880.5725 2018-06-26
DQA Oximeter Cardiovascular Class 2 870.2700 2018-06-26
MEA Pump, Infusion, Pca General Hospital Class 2 880.5725 2017-05-10

Official Correspondent

Christopher Enger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Med One Equipment Services
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
K913718 Abbott Laboratories PANCRETEC I.V. MODEL 5000 INFUS DEVICE, MODIFIED 1991-10-30
K840616 Advanced Bio Systems, Inc. MINI-PUMP U-100 1984-03-30
K850183 Deltec Systems, Inc. CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M 1985-03-13
K142467 Abeon Medical Corporation IntelAir Nasal Airway Support System 2014-11-24
K861213 Datex Division Instrumentarium Corp. PB 254 IR - SPECTROMETER 1986-04-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Single Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product Codes: 2M8151, 2M8161, and 2M9161.
Z-0002-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Triple Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product codes: 2M8153, and 2M8163.
Z-0005-2025 Zyno Medical LLC 2
Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
Z-0006-2011 CareFusion Corporation 2
CareFusion Alaris PC Unit Model 8015 (formerly Medley PC Unit): Alaris PC Units (Model 8015) with logic board part number TC10005522 manufactured and serviced between December 20, 2008 and May 6, 2009; and Alaris PC Units (with logic board part number TC10005572 manufactured and serviced between May 7, 2009 and September 8, 2009. For use with Alaris infusion and monitoring systems.
Z-0007-2012 B Braun Medical, Inc 2
Outlook ES Safety Infusion System, Model 621-100ES, 621-200ES, 621-300ES, and 621-400ES B. Braun Medical Inc., 1601 Wallace Drive, Suite 150, Carrollton, TX 75006 The Outlook ES pump is intended for use with B. Braun Medical Inc., Horizon Pump IV Sets to regulate the flow of primary and secondary fluids when positive pressure is required.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013652261. Last updated year: 2026. Please use registration number 3013652261 when referencing this establishment in official correspondence.
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