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Sign in to claim this brandBOUND TREE MEDICAL, LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2911 S GREAT SW PARKWAY, Grand Prairie, TX, 75052
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020460367
- DUNS Number
- —
Catalogue (2165)
Page 37 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01470 | FDA UDI | Class II | Active |
| Curaplex | 301-192 | FDA UDI | Class I | Active |
| Curaplex | 8600-01436 | FDA UDI | Class II | Active |
| Curaplex | 36627 | FDA UDI | Class II | Active |
| Curaplex | 8600-01326 | FDA UDI | Class I | Active |
| Curaplex | B903 | FDA UDI | Class I | Active |
| Curaplex | 5114ET | FDA UDI | Class II | Active |
| Curaplex | 2909006XL | FDA UDI | Class II | Active |
| Curaplex | 670204-KITFBA | FDA UDI | Class I | Active |
| Curaplex | SIVSTGAHP-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01249 | FDA UDI | Class II | Active |
| Curaplex | 8600-01257 | FDA UDI | Class II | Active |
| Curaplex | 2113-20280 | FDA UDI | Class II | Active |
| Curaplex | 670103-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01346 | FDA UDI | Class II | Active |
| Curaplex | 670127-KIT | FDA UDI | Class II | Active |
| Curaplex | BT-42610 | FDA UDI | Class I | Active |
| Curaplex | 8600-HMEKIT | FDA UDI | Class II | Active |
| Curaplex | 533-MS-YK50EA | FDA UDI | Class II | Active |
| Curaplex | 3310-14192 | FDA UDI | Class II | Active |
| Curaplex | 5714F-SE | FDA UDI | Class II | Active |
| Curaplex | 2021-15126 | FDA UDI | Class I | Active |
| Curaplex | 30055 | FDA UDI | Class II | Active |
| Curaplex | 3272-53578 | FDA UDI | Class I | Active |
| Curaplex | 661136 | FDA UDI | Class I | Active |
| Curaplex | 3250 | FDA UDI | Class I | Active |
| Curaplex | 8600-01143 | FDA UDI | Class II | Active |
| Curaplex | 660788-R-CAT | FDA UDI | Class I | Active |
| Curaplex | 2811-05522 | FDA UDI | Class I | Active |
| Curaplex | 8600-NRBPED-1594 | FDA UDI | Class I | Active |
| Curaplex | 5590 | FDA UDI | Class I | Active |
| Curaplex | 5114F-SE-E | FDA UDI | Class II | Active |
| Curaplex | 5207F-SE | FDA UDI | Class II | Active |
| Curaplex | 8600-01275 | FDA UDI | Class II | Active |
| Curaplex | 38013 | FDA UDI | Class II | Active |
| Curaplex | 8600-01489 | FDA UDI | Class II | Active |
| Curaplex | 62241163S | FDA UDI | Class II | Active |
| Curaplex | 670164-kit | FDA UDI | Class II | Active |
| Curaplex | 2021-15114 | FDA UDI | Class I | Active |
| Curaplex | 670264-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01292 | FDA UDI | Class II | Active |
| Curaplex | 670143-KIT | FDA UDI | Class II | Active |
| Curaplex | 670237-KIT | FDA UDI | Class II | Active |
| Curaplex | TC-MMCB2CG1A1GBBT | FDA UDI | Class I | Active |
| Curaplex | 1310-15203 | FDA UDI | N | Active |
| Curaplex | SFA100P-23-KIT | FDA UDI | Class I | Active |
| Curaplex | 30062 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-24101EA | FDA UDI | Class I | Active |
| Curaplex | 670213-KIT | FDA UDI | Class II | Active |
| Curaplex | 30078 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 14, 2020 | Z-2532-2020 | — | terminated | 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 |