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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 35 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 301-670254-KIT | FDA UDI | Class I | Active |
| Curaplex | 36613 | FDA UDI | Class II | Active |
| Curaplex | 670216-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01102 | FDA UDI | Class II | Active |
| Curaplex | B2110 | FDA UDI | Class I | Active |
| Curaplex | 8600-01423 | FDA UDI | Class II | Active |
| Curaplex | 36091 | FDA UDI | Class II | Active |
| Curaplex | 8600-01427 | FDA UDI | Class I | Active |
| Curaplex | S1137 | FDA UDI | Class I | Active |
| Curaplex | 3007 | FDA UDI | Class I | Active |
| Curaplex | 2114-19301 | FDA UDI | Class I | Active |
| Curaplex | 1121-36225 | FDA UDI | Class I | Active |
| Curaplex | 38019 | FDA UDI | Class II | Active |
| Curaplex | 301-PrO2LT | FDA UDI | Class II | Active |
| Curaplex | 2525-36703 | FDA UDI | Class I | Active |
| Curaplex | 658050 | FDA UDI | Class I | Active |
| Curaplex | 8600-01336 | FDA UDI | Class II | Active |
| Curaplex | 8600-01237 | FDA UDI | Class I | Active |
| Curaplex | TA3001 | FDA UDI | Class I | Active |
| Curaplex | 1212-12105 | FDA UDI | Class I | Active |
| Curaplex | 5214F-SE | FDA UDI | Class II | Active |
| Curaplex | 660786-CAT | FDA UDI | Class I | Active |
| Curaplex | 6872-POST | FDA UDI | Class II | Active |
| Curaplex | STB003A-XT | FDA UDI | Class I | Active |
| Curaplex | 8600-01233 | FDA UDI | Class I | Active |
| Curaplex | 36107-TVH | FDA UDI | Class II | Active |
| Curaplex | 8600-01199 | FDA UDI | Class II | Active |
| Curaplex | 29220S | FDA UDI | Class I | Active |
| Curaplex | 1012-47139 | FDA UDI | Class I | Active |
| Curaplex | 12328 | FDA UDI | Class I | Active |
| Curaplex | SEECRIC | FDA UDI | Class II | Active |
| Curaplex | 5107F-SE-E | FDA UDI | Class II | Active |
| Curaplex | TC-SMCB2NN1NE0GABA | FDA UDI | Class I | Active |
| Curaplex | 670228-KIT | FDA UDI | Class II | Active |
| Curaplex | 670245-KIT | FDA UDI | Class II | Active |
| Curaplex | 670185-KIT | FDA UDI | Class I | Active |
| Curaplex | 1715-01827 | FDA UDI | Class II | Active |
| Curaplex | 3271-62602 | FDA UDI | Class I | Active |
| Curaplex | 1121-36558 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-001PMP | FDA UDI | Class I | Active |
| Curaplex | 18269 | FDA UDI | Class II | Active |
| Curaplex® | 8600-01527 | FDA UDI | Class II | Active |
| Curaplex | TC3CB-B-HL-CAT | FDA UDI | Class I | Active |
| Curaplex | 301-LED-WH2-S | FDA UDI | Class I | Active |
| Curaplex | 2114-163015 | FDA UDI | Class I | Active |
| Curaplex | 2113-20240 | FDA UDI | Class II | Active |
| Curaplex | 680152-KIT | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 16353 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-3-S | 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 |