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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 17 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01317-10NAL | FDA UDI | Class I | Active |
| Curaplex | 2811-05523 | FDA UDI | Class I | Active |
| Curaplex | IBL1011 | FDA UDI | Class I | Active |
| Curaplex | 670161-kit | FDA UDI | Class II | Active |
| Curaplex | 301-182U | FDA UDI | Class I | Active |
| Curaplex | 777557 | FDA UDI | Class II | Active |
| Curaplex | EMP4000RC | FDA UDI | Class I | Active |
| Curaplex | 590412 | FDA UDI | Class I | Active |
| Curaplex | 1460-002QM | FDA UDI | Class I | Active |
| Curaplex | 2113-20330 | FDA UDI | Class II | Active |
| Curaplex | EMP3250GC-C | FDA UDI | Class I | Active |
| Curaplex | 8600-01148 | FDA UDI | Class II | Active |
| Curaplex | 670035-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-20290 | FDA UDI | Class II | Active |
| Curaplex | 301-140EA | FDA UDI | Class I | Active |
| Curaplex | TC3B-A-HL-CAT | FDA UDI | Class I | Active |
| Curaplex | 1121-36564 | FDA UDI | Class I | Active |
| Curaplex | 10-83611 | FDA UDI | Class II | Active |
| Curaplex | 2114-11001 | FDA UDI | Class II | Active |
| Curaplex | 2741-50484 | FDA UDI | Class II | Active |
| Curaplex | 2113-20295 | FDA UDI | Class II | Active |
| Curaplex | 36158 | FDA UDI | Class II | Active |
| Curaplex | 8600-ACSTWN-12110 | FDA UDI | Class I | Active |
| Curaplex | 2525-31601 | FDA UDI | Class II | Active |
| Curaplex | SEEFRKITGA | FDA UDI | Class I | Active |
| Curaplex | 1012-47125 | FDA UDI | Class I | Active |
| Curaplex | NC100 | FDA UDI | Class I | Active |
| Curaplex | 8600-01197 | FDA UDI | Class I | Active |
| Curaplex | 2515-01104 | FDA UDI | Class II | Active |
| Curaplex | 38014 | FDA UDI | Class II | Active |
| Curaplex | 440414OD | FDA UDI | Class I | Active |
| Curaplex | 8600-01251 | FDA UDI | Class II | Active |
| Curaplex | 3245-19123 | FDA UDI | Class I | Active |
| Curaplex | 8600-ETTB70-1269 | FDA UDI | Class II | Active |
| Curaplex | 661129 | FDA UDI | Class I | Active |
| Curaplex | 444001 | FDA UDI | Class II | Active |
| Curaplex | EMPX | FDA UDI | Class I | Active |
| Curaplex | 8600-01443 | FDA UDI | Class I | Active |
| Curaplex | 670018-KIT | FDA UDI | Class I | Active |
| Curaplex | 670026-KIT | FDA UDI | Class I | Active |
| Curaplex | 16381 | FDA UDI | Class II | Active |
| Curaplex | GP126 | FDA UDI | Class I | Active |
| Curaplex | 1012-47141 | FDA UDI | Class I | Active |
| Curaplex | 8600-01294 | FDA UDI | Class II | Active |
| Curaplex | 1004SPF | FDA UDI | Class II | Active |
| Curaplex | 8600-01336 | FDA UDI | Class II | Active |
| Curaplex | 2741-50487 | FDA UDI | Class II | Active |
| Curaplex | 8600-01501 | FDA UDI | Class II | Active |
| Curaplex | B4024 | FDA UDI | Class I | Active |
| Curaplex | 1841-14009 | FDA UDI | Class I | 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 |