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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 43 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1612-84245 | FDA UDI | Class II | Active |
| Curaplex | 14758MS | FDA UDI | Class II | Active |
| Curaplex | 1121-36645 | FDA UDI | Class I | Active |
| Curaplex | 661130 | FDA UDI | Class I | Active |
| Curaplex | 8600-01458 | FDA UDI | Class II | Active |
| Curaplex | 44260 | FDA UDI | Class II | Active |
| Curaplex | 2741-50485 | FDA UDI | Class II | Active |
| Curaplex | 36153 | FDA UDI | Class II | Active |
| Curaplex | B900 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4670 | FDA UDI | Class I | Active |
| Curaplex | 662177 | FDA UDI | Class I | Active |
| Curaplex | 670188-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01508 | FDA UDI | Class I | Active |
| Curaplex | 262091P | FDA UDI | Class I | Active |
| Curaplex | 8600-01474 | FDA UDI | Class I | Active |
| Curaplex | 670278-KIT | FDA UDI | Class I | Active |
| Curaplex | 023060S | FDA UDI | Class II | Active |
| Curaplex | 1860-08708BR | FDA UDI | Class II | Active |
| Curaplex | 301-P3050 | FDA UDI | Class II | Active |
| Curaplex | 2-0211-8136 | FDA UDI | Class I | Active |
| Curaplex | 441403 | FDA UDI | Class I | Active |
| Curaplex | B701 | FDA UDI | Class I | Active |
| Curaplex | 1715-01837 | FDA UDI | Class II | Active |
| Curaplex | 8600-01225 | FDA UDI | Class II | Active |
| Curaplex | 028055 | FDA UDI | Class I | Active |
| Curaplex | 1212-12104 | FDA UDI | Class I | Active |
| Curaplex | 1212-12110 | FDA UDI | Class I | Active |
| Curaplex | NC201 | FDA UDI | Class I | Active |
| Curaplex | 2113-10285 | FDA UDI | Class II | Active |
| Curaplex | FCBLF-NVY | FDA UDI | Class I | Active |
| Curaplex | 670132-KIT | FDA UDI | Class II | Active |
| Curaplex | 1121-36547 | FDA UDI | Class I | Active |
| Curaplex | 36094 | FDA UDI | Class II | Active |
| Curaplex | 670155-KIT | FDA UDI | Class II | Active |
| Curaplex | 777556-1 | FDA UDI | Class II | Active |
| Curaplex | 8600-01507 | FDA UDI | Class I | Active |
| Curaplex | 2113-10245 | FDA UDI | Class II | Active |
| Curaplex | 8600-01124 | FDA UDI | Class II | Active |
| Curaplex | QASEEPNEK | FDA UDI | Class II | Active |
| Curaplex | 36154 | FDA UDI | Class II | Active |
| Curaplex | 3141-91014 | FDA UDI | Class I | Active |
| Curaplex | 36741 | FDA UDI | Class I | Active |
| Curaplex | 301-181U | FDA UDI | Class I | Active |
| Curaplex | 8600-VILADP-1434 | FDA UDI | Class II | Active |
| Curaplex | 670177-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01269 | FDA UDI | Class I | Active |
| Curaplex | 1212-12115 | FDA UDI | Class I | Active |
| Curaplex | 71051 | FDA UDI | Class II | Active |
| Curaplex | 8600-01331 | FDA UDI | Class I | Active |
| Curaplex | 2114-04086-KIT | 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 |