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Data / Medical devices / Mexico / Rci Hudson De Mexico S. De RL. De CV.

Rci Hudson De Mexico S. De RL. De CV.: FDA-registered device maker in Nuevo Laredo Tamaulipas, Mexico, 38 510(k) clearances

Rci Hudson De Mexico S. De RL. De CV. is registered with the FDA (registration 3029706818) in Nuevo Laredo Tamaulipas, Mexico. It lists 24 device types. The FDA files 38 510(k) clearances under its listings, the newest dated March 25, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch Rci Hudson De Mexico S. De RL. De CV.
FDA registration number
3029706818
Address
Av. Industrias No. 5902, Building 2 Parque Industrial FINSA, Nuevo Laredo Tamaulipas, Mexico, 88275
Owner or operator
Medline Industries, LP (1417592)
Roles
Manufacturer
First device listed
October 1, 1979
Registered through
2026
Brand names listed
"Salt Airway S.A.L.T.", Angio-SAC Collection System, AquaPak Humidifier Adapters, Aquapak Humidifier Reservoir with Adaptor, Aquapak Nebulizer Reservoir with Adaptor, Aquapak Nebulizer; Aquapak Saline Reservoir; Aquapak Sterile Water Reservoir, Aquapak Sterile Humidifier Reservoirs, BERMAN AIRWAYS and more

Devices it lists

DeviceProduct codeClassRoleSource
Airway, Oropharyngeal, AnesthesiologyCAE1Manufactureraccessdata.fda.gov
Cannula, Nasal, OxygenCAT1Manufactureraccessdata.fda.gov
Catheter, Intravascular, DiagnosticDQO2Manufactureraccessdata.fda.gov
Catheter, Nasal, OxygenBZB1Manufactureraccessdata.fda.gov
Circuit, Breathing (W Connector, Adaptor, Y Piece)CAI1Manufactureraccessdata.fda.gov
Connector, Airway (Extension)BZA1Manufactureraccessdata.fda.gov
Device, Fixation, Tracheal TubeCBH1Manufactureraccessdata.fda.gov
Drain, Tee (Water Trap)BYH1Manufactureraccessdata.fda.gov
Endoscopic Bite BlockMNK1Manufactureraccessdata.fda.gov
Heater, Breathing System W/Wo Controller (Not Humidifier Or NebulizerBZE2Manufactureraccessdata.fda.gov
Humidifier Nebulizer KitOGG2Manufactureraccessdata.fda.gov
Humidifier, Respiratory Gas, (Direct Patient Interface)BTT2Manufactureraccessdata.fda.gov
Mask, OxygenBYG1Manufactureraccessdata.fda.gov
Mask, Oxygen, Low Concentration, VenturiBYF1Manufactureraccessdata.fda.gov
Mask, Oxygen, Non-RebreathingKGB1Manufactureraccessdata.fda.gov
Mouthpiece, BreathingBYP1Manufactureraccessdata.fda.gov
Nebulizer (Direct Patient Interface)CAF2Manufactureraccessdata.fda.gov
Regulator, Pressure, Gas CylinderCAN1Manufactureraccessdata.fda.gov
Set, Administration, IntravascularFPA2Manufactureraccessdata.fda.gov
Set, Tubing And Support, Ventilator (W Harness)BZO1Manufactureraccessdata.fda.gov
Spirometer, Therapeutic (Incentive)BWF2Manufactureraccessdata.fda.gov
Thermometer, Clinical Color ChangeFQZ1Manufactureraccessdata.fda.gov
Tubing, Pressure And AccessoriesBYX1Manufactureraccessdata.fda.gov
Ventilator, Non-Continuous (Respirator)BZD2Manufactureraccessdata.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
March 25, 2026K253322Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with 78” Infant Circuit, HUD99060KIT / Dri-Tech with 78” Infant Circuit Kit, HUD99001KIT / Single Limb Infant Circuit Dri-Tech Kit, HUD99009KIT / Dri-Tech with 60” Infant Circuit Kit, HUD99018KIT / Dri-Tech with 44” Infant Circuit Kit, HUD870NKIT / Dri-Tech Infant Accessory Bag, HUD1631 / Infant Wye Connector with Swivel)BZESubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
July 2, 2025K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra SmallBTTSubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
December 19, 2024K241778Hudson RCI Comfort Flo® CubCannula™BTTSubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
September 27, 2024K240163Hudson RCI® Comfort Flo Nasal Cannula; Hudson RCI® Comfort Flo Plus CannulaBTTSubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
June 4, 2024K234032Hudson RCI Dri-Tech Breathing Circuits; HUD99035/Dri-Tech Adult Circuit; HUD99035KIT/Dri-Tech Adult Circuit Kit; HUD99098KIT/Single Limb Adult Dri-Tech Kit; HUD99098KITF/Single Limb Adult Dri-Tech Filter Kit; HUD900/Dri-Tech Ventilator Accessory; HUD901/Dri-Tech Ventilator Accessory Extension LineBZESubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
October 31, 2023K230602Hudson RCI® TurboMist™ Nebulizer SystemCAFSubstantially EquivalentMedline Industries, LPaccessdata.fda.gov
October 26, 2023K230559Hudson RCI® Disposable Humidifier with 4 PSI Pressure Relief Valve (3230), Hudson RCI® Disposable Humidifier with 6 PSI Pressure Relief Valve (3260)BTTSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
June 27, 2023K223100Hudson RCI AquaTherm III Plus External Adjustable Electronic Heater (050-14)CAFSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
June 23, 2023K220955Hudson RCI Variable concentration Large Volume Nebulizer (1770)CAFSubstantially EquivalentMedline Industires, Inc.accessdata.fda.gov
October 25, 2022K220565Hudson RCI Triflo II Incentive Deep Breathing ExerciserBWFSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
July 1, 2019K182847Hudson RCI Voldyne Volumetric ExerciserBWFSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
January 19, 2017K162242Comfort Flo Humidification SystemBTTSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
July 26, 2016K153010Hudson RCI AquaPak Sterile Prefilled NebulizersCAFSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
December 18, 2014K141214AQUAPAK NEBULIZER ADAPTORS/RESERVOIRSCAFSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
November 24, 2014K141940CONCHASMART COLUMNBTTSubstantially EquivalentTeleflex, Inc.accessdata.fda.gov
September 24, 2014K140556CONCHASMART BREATHING CIRCUITBTTSubstantially EquivalentTeleflex, Inc.accessdata.fda.gov
August 1, 2014K141353HUDSON RCI AQUAPAK HUMIDIFIER ADAPTORBTTSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
March 6, 2014K131912CONCHATHERM NEPTUNE HEATED HUMIDIFIER, COMFORT FLO HUMIDIFICATION SYSTEM, CONCHASMART COLUMNBTTSubstantially EquivalentTeleflex, Inc.accessdata.fda.gov
June 9, 2008K080230NEB-U-MASK SYSTEM, MODELS 1895, 1896CAFSubstantially EquivalentTeleflexmedical, Inc.accessdata.fda.gov
April 23, 2007K063758CHONCHA THERM NEPTUNE HEATED HUMIFIER, CHONCHA THERM NEPTUNE HEATED HUMIFIER (REMANUFACTURER), MODEL# 425-00,425-00RBTTSubstantially EquivalentTeleflex Medicalaccessdata.fda.gov
July 7, 2003K031383MODEL 780BTTSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
March 14, 2001K010402SMOOTH-FLO CIRCUITBTTSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
November 3, 2000K001213CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60BTTSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
March 22, 2000K994352SIDE DRAFT NEB-U-MIST NEBULIZER, MODEL 41896CAFSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
September 14, 1998K982408AEROTEE, MODEL # 1001CAFSubstantially EquivalentPiper Medical Productsaccessdata.fda.gov
September 29, 1993K930525MICRO MIST(TM) NEBULIZERCAFSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
December 27, 1990K903083NEONATAL VENTILATOR CIRCUITBZOSubstantially EquivalentHudson Respiratory Care, Inc.accessdata.fda.gov
July 18, 1990K900783MDI ADAPTORCAFSubstantially EquivalentHudson Oxygen Therapy Sales Co.accessdata.fda.gov
October 27, 1989K895231CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZERCAFSubstantially EquivalentHudson Oxygen Therapy Sales Co.accessdata.fda.gov
June 21, 1988K881625CONCHATHERM III PLUS DUAL HEAT WIRE SERVO CONTROLLBZESubstantially EquivalentRespiratory Care, Inc.accessdata.fda.gov
April 21, 1987K871157C.P.A.P. NASAL CANNULABZDSubstantially EquivalentHudson Oxygen Therapy Sales Co.accessdata.fda.gov
May 30, 1985K852140NAMIC CONTRAST & FLUID DELIVERY SPIKES(VARIOUS)FPASubstantially EquivalentNorth American Instrument Corp.accessdata.fda.gov
October 18, 1984K843726NAMIC ADB ANGIOGRAPHIC DUMP BAGDQOSubstantially EquivalentNorth American Instrument Corp.accessdata.fda.gov
May 3, 1982K820878CONCHO PEDIATRIC PACKBTTSubstantially EquivalentRci, Inc.accessdata.fda.gov
June 4, 1980K801199VOLDYNE VOLUMETRIC INCENTIVE DEEP BR. EXBWFSubstantially EquivalentChesebrough-Pond'S U.S.A. Co.accessdata.fda.gov
December 15, 1978K781831SPIROMETER, INCENTIVE CATALOG # 1750BWFSubstantially EquivalentHudson Oxygen Therapy Sales Co.accessdata.fda.gov
November 1, 1976K760866CONCHA-COLUMNBTTSubstantially EquivalentRespiratory Care, Inc.accessdata.fda.gov
September 3, 1976K760489NEBULIZER, HANDHELD (T UP-DRAFT)CAFSubstantially EquivalentHudson Oxygen Therapy Sales Co.accessdata.fda.gov

Compare with other makers

Updated March 25, 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.