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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 7 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2113-20275 | FDA UDI | Class II | Active |
| Curaplex | 670257-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-182EA | FDA UDI | Class I | Active |
| Curaplex® | SIVSTTCF-24-KIT | FDA UDI | Class II | Active |
| Curaplex | TC2B-I-ML-ST | FDA UDI | Class I | Active |
| Curaplex® | 3271-63403 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-WH15-M | FDA UDI | Class I | Active |
| Curaplex | 1471-32000 | FDA UDI | Class II | Active |
| Curaplex | B3210EA | FDA UDI | Class I | Active |
| Curaplex | 8600-01341 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-104S | FDA UDI | Class I | Active |
| Curaplex | 8600-01367 | FDA UDI | Class I | Active |
| Curaplex | 2760 | FDA UDI | Class I | Active |
| Curaplex | B801 | FDA UDI | Class I | Active |
| Curaplex | 1431-16000 | FDA UDI | Class I | Active |
| Curaplex | 2113-10255 | FDA UDI | Class II | Active |
| Curaplex | 670093-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-141EA | FDA UDI | Class I | Active |
| Curaplex | 5107ET-E | FDA UDI | Class II | Active |
| Curaplex | 1860-08700 | FDA UDI | Class II | Active |
| Curaplex | 8600-01406 | FDA UDI | Class II | Active |
| Curaplex | 51089 | FDA UDI | Class II | Active |
| Curaplex | 683922 | FDA UDI | Class II | Active |
| Curaplex | 1612-84220 | FDA UDI | Class II | Active |
| Curaplex | 2113-20285 | FDA UDI | Class II | Active |
| Curaplex | 670251-KIT | FDA UDI | Class II | Active |
| Curaplex | 531502P | FDA UDI | Class I | Active |
| Curaplex | 2811-05528 | FDA UDI | Class I | Active |
| Curaplex | STB003A-SOFTT | FDA UDI | Class I | Active |
| Curaplex | 301-142 | FDA UDI | Class I | Active |
| Curaplex | 3271-44150EP | FDA UDI | Class I | Active |
| Curaplex | 12945 | FDA UDI | Class I | Active |
| Curaplex | 8600-01112 | FDA UDI | Class I | Active |
| Curaplex | 670064-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-SG1MLS-1437 | FDA UDI | Class II | Active |
| Curaplex | 14762MS | FDA UDI | Class II | Active |
| Curaplex | 8600-01514 | FDA UDI | Class II | Active |
| Curaplex | 8600-01433 | FDA UDI | Class I | Active |
| Curaplex | 8600-01205 | FDA UDI | Class II | Active |
| Curaplex | 2010-34070 | FDA UDI | Class I | Active |
| Curaplex | 8600-01212 | FDA UDI | Class II | Active |
| Curaplex | 14761 | FDA UDI | Class II | Active |
| Curaplex | 8600-ETTB45-1264 | FDA UDI | Class II | Active |
| Curaplex | 2114-13003 | FDA UDI | Class II | Active |
| Curaplex | 1714-32210 | FDA UDI | Class II | Active |
| Curaplex | 670144-KIT | FDA UDI | Class II | Active |
| Curaplex | 670209-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01361 | FDA UDI | Class I | Active |
| Curaplex | 8600-01305 | FDA UDI | Class I | Active |
| Curaplex | NC202 | 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 |