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Data / Medical devices / United States / Ups Supply Chain Solutions, Inc.

Ups Supply Chain Solutions, Inc.: FDA-registered device maker in Louisville, KY, United States, 28 510(k) clearances and 4 PMA approvals

Ups Supply Chain Solutions, Inc. is registered with the FDA (registration 3009171251) in Louisville, KY, United States. It lists 62 device types. The FDA files 28 510(k) clearances and 4 PMA approvals under its listings, the newest dated August 16, 2024. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Ups Supply Chain Solutions, Inc.
FDA registration number
3009171251
FEI number
3006759904
Address
1860 Outer Loop, Louisville, KY, United States, 40219
Owner or operator
UPS SUPPLY CHAIN SOLUTIONS, INC. (9073670)
Roles
Repackager or relabeler
First device listed
June 22, 2011
Registered through
2026
Brand names listed
1 LITER RAINBOW BREATHING BAG®, 12" NAFION LINE, 2 LITER CONTOUR®, 2 LITER RAINBOW BREATHING BAG®, 22MM X 22MM I.D. ADAPTER, 24" NAFION LINE, 5" 15MM ULTRA FLEX® TUBING, 6" NAFION TUBING and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, CatheterKGZ1Repackager or relabeleraccessdata.fda.gov
Airway, Oropharyngeal, AnesthesiologyCAE1Repackager or relabeleraccessdata.fda.gov
Attachment, Breathing, Positive End Expiratory PressureBYE2Repackager or relabeleraccessdata.fda.gov
Automated Antimicrobial Susceptibility Test System For Positive Blood Culture SamplesSAN2Repackager or relabeleraccessdata.fda.gov
Automated Insulin Dosing , Threshold SuspendOZO3Repackager or relabeleraccessdata.fda.gov
Automated Insulin Dosing Device System, Single Hormonal ControlOZP3Repackager or relabeleraccessdata.fda.gov
Bag, ReservoirBTC1Repackager or relabeleraccessdata.fda.gov
Bronchoscope (Flexible Or Rigid)EOQ2Repackager or relabeleraccessdata.fda.gov
Catheter, UrologicalKOD2Repackager or relabeleraccessdata.fda.gov
Circuit, Breathing (W Connector, Adaptor, Y Piece)CAI1Repackager or relabeleraccessdata.fda.gov
Condenser, Heat And Moisture (Artificial Nose)BYD1Repackager or relabeleraccessdata.fda.gov
Connector, Airway (Extension)BZA1Repackager or relabeleraccessdata.fda.gov
Container, Specimen, SterileFMH1Repackager or relabeleraccessdata.fda.gov
Culture Media, Non-Selective And Non-DifferentialJSG1Repackager or relabeleraccessdata.fda.gov
Cystoscope And Accessories, Flexible/RigidFAJ2Repackager or relabeleraccessdata.fda.gov
Device, Monitoring, Intracranial PressureGWM2Repackager or relabeleraccessdata.fda.gov
Discs, Strips And Reagents, Microorganism DifferentiationJTO1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, DrugFROURepackager or relabeleraccessdata.fda.gov
Dressing, Wound, OcclusiveNAD1Repackager or relabeleraccessdata.fda.gov
Duodenoscope And Accessories, Flexible/RigidFDT2Repackager or relabeleraccessdata.fda.gov
Electrode, CutaneousGXY2Repackager or relabeleraccessdata.fda.gov
Electrode, ElectrocardiographDRX2Repackager or relabeleraccessdata.fda.gov
Electrode, NeedleGXZ2Repackager or relabeleraccessdata.fda.gov
Electrode, Needle, Diagnostic ElectromyographIKT2Repackager or relabeleraccessdata.fda.gov
Endoscopic Video Imaging System/Component, Gastroenterology-UrologyFET2Repackager or relabeleraccessdata.fda.gov
Enzyme Linked Immunoabsorbent Assay, Mumps VirusLJY1Repackager or relabeleraccessdata.fda.gov
Enzyme Linked Immunoabsorbent Assay, Rubeola IggLJB1Repackager or relabeleraccessdata.fda.gov
Filter, Bacterial, Breathing-CircuitCAH2Repackager or relabeleraccessdata.fda.gov
Gastroscope And Accessories, Flexible/RigidFDS2Repackager or relabeleraccessdata.fda.gov
Glucose Dehydrogenase, GlucoseLFR2Repackager or relabeleraccessdata.fda.gov
Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsQLG2Repackager or relabeleraccessdata.fda.gov
Kit, Identification, EnterobacteriaceaeJSS1Repackager or relabeleraccessdata.fda.gov
Kit, Identification, YeastJXB1Repackager or relabeleraccessdata.fda.gov
Mask, Gas, AnestheticBSJ1Repackager or relabeleraccessdata.fda.gov
Mask, OxygenBYG1Repackager or relabeleraccessdata.fda.gov
Medical Device Data SystemOUG1Repackager or relabeleraccessdata.fda.gov
Monitor, Airway Pressure (Includes Gauge And/Or Alarm)CAP2Repackager or relabeleraccessdata.fda.gov
Multiple Use Blood Lancet For Single Patient Use OnlyQRL2Repackager or relabeleraccessdata.fda.gov
Nasopharyngoscope (Flexible Or Rigid)EOB2Repackager or relabeleraccessdata.fda.gov
Nitroprusside, Ketones (Urinary, Non-Quant.)JIN1Repackager or relabeleraccessdata.fda.gov
Orthosis, CervicalIQK1Repackager or relabeleraccessdata.fda.gov
Panels, Test, Susceptibility, AntimicrobialLTT2Repackager or relabeleraccessdata.fda.gov
Pump, Infusion, ElastomericMEB2Repackager or relabeleraccessdata.fda.gov
Reagents, Clostridium Difficile ToxinLLH1Repackager or relabeleraccessdata.fda.gov
Sensor, Glucose, InvasiveMDS3Repackager or relabeleraccessdata.fda.gov
Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-InitiatedPZE3Repackager or relabeleraccessdata.fda.gov
Set, Tubing And Support, Ventilator (W Harness)BZO1Repackager or relabeleraccessdata.fda.gov
Single (Specified) Analyte Controls (Assayed And Unassayed)JJX1Repackager or relabeleraccessdata.fda.gov
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK2Repackager or relabeleraccessdata.fda.gov
Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention FeatureQRK2Repackager or relabeleraccessdata.fda.gov
Strap, Head, Gas MaskBTK1Repackager or relabeleraccessdata.fda.gov
Support, Patient PositionCCX1Repackager or relabeleraccessdata.fda.gov
Susceptibility Test Cards, AntimicrobialLTW2Repackager or relabeleraccessdata.fda.gov
System, Mass Spectrometry, Maldi Tof, Microorganism Identification, Cultured IsolatesPEX2Repackager or relabeleraccessdata.fda.gov
System, Photopheresis, ExtracorporealLNR3Repackager or relabeleraccessdata.fda.gov
System, Rebreathing, RadionuclideIYT2Repackager or relabeleraccessdata.fda.gov
System, Test, Automated, Antimicrobial Susceptibility, Short IncubationLON2Repackager or relabeleraccessdata.fda.gov
System, Test, Blood Glucose, Over The CounterNBW2Repackager or relabeleraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Repackager or relabeleraccessdata.fda.gov
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)CBI2Repackager or relabeleraccessdata.fda.gov
Tubing, Pressure And AccessoriesBYX1Repackager or relabeleraccessdata.fda.gov
Ureteroscope And Accessories, Flexible/RigidFGB2Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 16, 2024K242108Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aView™ 2 AdvanceFGBSubstantially EquivalentAmbu A/Saccessdata.fda.gov
June 20, 2024K230675VITEK REVEAL GN AST Assay and VITEK REVEAL AST SystemSANSubstantially EquivalentSpecific Diagnostics, LLCaccessdata.fda.gov
April 16, 2024K233886Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2FDTSubstantially EquivalentAmbu A/Saccessdata.fda.gov
July 15, 2022K221433Facet 28G Universal LancetQRKSubstantially EquivalentFacet Technologies, LLCaccessdata.fda.gov
May 26, 2022K212132FreeStyle Libre 3 Continuous Glucose Monitoring SystemQLGSubstantially EquivalentAbbott Diabetes Care, Inc.accessdata.fda.gov
February 3, 2022K212382Ambu® aScope™ Gastro, Ambu® aBox™2FDSSubstantially EquivalentAmbu A/Saccessdata.fda.gov
May 3, 2021K203749Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter CableCBISubstantially EquivalentAmbu A/Saccessdata.fda.gov
June 12, 2020K193371FreeStyle Libre 2 Flash Glucose Monitoring SystemQLGSubstantially EquivalentAbbott Diabetes Care, Inc.accessdata.fda.gov
April 2, 2020K193095Ambu aScope 4 CystoFAJSubstantially EquivalentAmbu A/Saccessdata.fda.gov
May 22, 2019K191080Ambu aScope 4 RhinoLaryngo SlimEOBSubstantially EquivalentAmbu A/Saccessdata.fda.gov
March 7, 2019K183551VITEK 2 AST-Gram Negative Minocycline (<= 0.5 - >= 32 ug/mL)LONSubstantially EquivalentbioMerieux, Inc.accessdata.fda.gov
March 28, 2018K173727Ambu aScope 3 Slim 3.8/1.2 and Ambu aScope 4 Broncho Slim 3.8/1.2; Ambu aScope 3 Regular 5.0/2.2 and Ambu aScope 4 Broncho Regular 5.0/2.2; Ambu aScope 3 Large 5.8/2.8 and Ambu aScope 4 Broncho Large 5.8/2.8; Ambu aView MonitorEOQSubstantially EquivalentAmbu A/Saccessdata.fda.gov
July 22, 2017K162950VITEK MSPEXSubstantially EquivalentbioMerieux, Inc.accessdata.fda.gov
September 30, 2015K142928FreeStyle Precision Neo Blood Glucose Monitoring SystemNBWSubstantially EquivalentAbbott Diabetes Care, Inc.accessdata.fda.gov
December 20, 2010K102875CAMINO 110-4B OLM INTRACRANIAL PRESSURE MNITORING KIT; CAMINO 110-4G POST CRANIOTOMY SUBDURAL PRESSURE MONITORING KIT; CGWMSubstantially EquivalentIntegra LifeSciences Corporationaccessdata.fda.gov
December 16, 2009K091034AQUACEL AG SURGICALFROSubstantially EquivalentConvatecaccessdata.fda.gov
August 21, 2007K063729DISPOSABLE PEDICLE SCREW PROBE, MODEL 3603-00GXZSubstantially EquivalentTechnomed Europeaccessdata.fda.gov
July 30, 2007K071186MODIFICATION TO: AMBU NEUROLINE CONCENTRIC NEEDLE ELECTRODEIKTSubstantially EquivalentAmbu A/Saccessdata.fda.gov
June 16, 2006K061409SMARTINFUSER PAINPUMP, MODEL P49220 W/CATHETER SET; P49224N W/O CATHETER SETMEBSubstantially EquivalentPrecise Medical Products, Ltd.accessdata.fda.gov
April 21, 2006K060768PRECISION XTRA BLOOD B KETONE TEST STRIPS, OPTIUM BLOOD B KETONE TEST STRIPSJINSubstantially EquivalentAbbott Diabetes Care, Inc.accessdata.fda.gov
May 27, 2005K051213PRECISION XTRA PLUS OR OPTIUM PLUS, BLOOD GLUCOSE TEST STRIPSNBWSubstantially EquivalentAbbott Laboratories, Inc.accessdata.fda.gov
July 22, 2004K040991AMBU DISPOSABLE PRESSURE MANOMETERCAPSubstantially EquivalentAmbu, Inc.accessdata.fda.gov
November 3, 1995K953513XENON CIRCUITIYTSubstantially EquivalentKing Systems Corp.accessdata.fda.gov
December 21, 1993K931430CUTANEOUS ELECTRODEGXYSubstantially EquivalentMedicotest, Inc.accessdata.fda.gov
December 21, 1993K931426NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODEGXYSubstantially EquivalentMedicotest, Inc.accessdata.fda.gov
January 5, 1993K923976AMBU SINGLE PATIENT USE PEEP VALVEBYESubstantially EquivalentAmbu, Inc.accessdata.fda.gov
November 5, 1990K896729NELATON-, FEMALE - OR TIEMANN CATHETERKODSubstantially EquivalentUnoplast A/Saccessdata.fda.gov
April 29, 1988K880681MINI-FILTER, VIROBAC IICAHSubstantially EquivalentKing Systems Corp.accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
September 27, 2017P160030Freestyle Libre Flash Glucose Monitoring SystemPZE54September 1, 2026accessdata.fda.gov
September 28, 2016P160017MiniMed 670G SystemOZP126September 29, 2026accessdata.fda.gov
June 17, 2016P150029IPRO2 CGM SYSTEM WITH ENLITE SENSORMDS36April 29, 2022accessdata.fda.gov
April 8, 1987P860003UVAR PHOTOPHERESIS SYSTEMLNR107November 21, 2025accessdata.fda.gov

Compare with other makers

Updated September 1, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.