Bound Tree Medical, LLC
Grand Prairie, TX, US
BOUND TREE MEDICAL, LLC appears in FDA device records in Grand Prairie, TX. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3020460367 | 3020460367 | BOUND TREE MEDICAL, LLC | 2911 S GREAT SW PARKWAY, Grand Prairie, TX 75052 US | 2026 | and 68 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KGZAccessories, Catheter
- MRZAccessories, Pump, Infusion
- LYUAccessory, Surgical Apparel
- OFOAirway Suction Kit
- CAOAirway, Esophageal (Obturator)
- BTQAirway, Nasopharyngeal
- CAEAirway, Oropharyngeal, Anesthesiology
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- CCTApplicator (Laryngo-Tracheal), Topical Anesthesia
- CBTArterial Blood Sampling Kit
- BYEAttachment, Breathing, Positive End Expiratory Pressure
- MKJAutomated External Defibrillators (Non-Wearable)
- FNYBasin, Emesis
- KMEBedding, Disposable, Medical
- GFABlade, Saw, General & Plastic Surgery, Surgical
- DXQBlood Pressure Cuff
- OFZBlood Specimen Collection Kit (Excludes Hiv Testing)
- KDQBottle, Collection, Vacuum
- CATCannula, Nasal, Oxygen
- OEVCardiopulmonary Resuscitation Aid Kit
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- LNZChanger, Tube, Endotracheal
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- MMKContainer, Sharps
- CFWCopper Reduction, Glucose
- FMRDevice, Transfer, Patient, Manual
- BYHDrain, Tee (Water Trap)
- DRXElectrode, Electrocardiograph
- LRRFirst Aid Kit With Drug
- NABGauze / Sponge,Nonresorbable For External Use
- BZEHeater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
- LRSI.V. Start Kit
- DXTInjector And Syringe, Angiographic
- CCWLaryngoscope, Rigid
- KGBMask, Oxygen, Non-Rebreathing
- CAFNebulizer (Direct Patient Interface)
- CCQNebulizer, Medicinal, Non-Ventilatory (Atomizer)
- FMINeedle, Hypodermic, Single Lumen
- DQAOximeter
- CANRegulator, Pressure, Gas Cylinder
- MSHRespirator, Surgical
- FMQRestraint, Protective
- NGTSaline, Vascular Access Flush
- FPASet, Administration, Intravascular
- BWFSpirometer, Therapeutic (Incentive)
- NZDStretcher, Patient Restraint
- FPOStretcher, Wheeled
- CCXSupport, Patient Position
- FMFSyringe, Piston
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
- KSZSystem, Test, Automated Blood Grouping And Antibody
- NBWSystem, Test, Blood Glucose, Over The Counter
- GAXTourniquet, Nonpneumatic
- BTRTube, Tracheal (W/Wo Connector)
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- CBPValve, Non-Rebreathing
- BTMVentilator, Emergency, Manual (Resuscitator)
- BTLVentilator, Emergency, Powered (Resuscitator)
- BZDVentilator, Non-Continuous (Respirator)
- MCYWound Dressing Kit
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-2532-2020 | Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part Number: KLTSD404K Curaplex Ambu King LTS-D" Supraglottic Airway Kit with ET Tube (hereafter the Kit which contains all of the components necessary to successfully obtain an open patient airway with an Ambu King LTS-D" Supraglottic Airway. | Kit contained an incorrect catheter-tip syringe not compatible with the luer lock connector of the included airway. As a result, may be unable to inflate the balloons of the supraglottic airway to create a secure seal in the patient s airway as intended by the kit | Class II | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain