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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
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020460367
- DUNS Number
- —
Catalogue (2165)
Page 31 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 36749 | FDA UDI | Class I | Active |
| Curaplex | 8600-01424 | FDA UDI | Class II | Active |
| Curaplex | 2113-10245 | FDA UDI | Class II | Active |
| Curaplex | 73320L | FDA UDI | Class II | Active |
| Curaplex | 301-LED-PH2-M | FDA UDI | Class I | Active |
| Curaplex | 2811-05526 | FDA UDI | Class I | Active |
| Curaplex | 2143-20404 | FDA UDI | Class I | Active |
| Curaplex | 36161 | FDA UDI | Class II | Active |
| Curaplex | 36101 | FDA UDI | Class II | Active |
| Curaplex | 8600-01483 | FDA UDI | Class II | Active |
| Curaplex | 290025 | FDA UDI | Class I | Active |
| Curaplex | 8600-01218 | FDA UDI | Class I | Active |
| Curaplex | 1071-11106 | FDA UDI | Class I | Active |
| Curaplex | 8600-LANCTS-1323 | FDA UDI | Class II | Active |
| Curaplex | 2-0211-4645 | FDA UDI | Class I | Active |
| Curaplex | 8600-01229 | FDA UDI | Class II | Active |
| Curaplex | 36183 | FDA UDI | Class II | Active |
| Curaplex | 1212-12108 | FDA UDI | Class I | Active |
| Curaplex | 8600-01451 | FDA UDI | Class II | Active |
| Curaplex | 2114-16303 | FDA UDI | Class I | Active |
| Curaplex | 8600-01256 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-2-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01510 | FDA UDI | Class I | Active |
| Curaplex | 38001 | FDA UDI | Class II | Active |
| Curaplex | 1612-84150 | FDA UDI | Class II | Active |
| Curaplex | 2022-35139 | FDA UDI | Class I | Active |
| Curaplex | 677555 | FDA UDI | Class II | Active |
| Curaplex | 670148-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01214 | FDA UDI | Class II | Active |
| Curaplex | STB001B-SOFTT | FDA UDI | Class I | Active |
| Curaplex® | 3271-63401 | FDA UDI | Class I | Active |
| Curaplex | 8600-01447 | FDA UDI | Class II | Active |
| Curaplex | 1121-36548 | FDA UDI | Class I | Active |
| Curaplex | 1510-77719 | FDA UDI | Class II | Active |
| Curaplex | 2021-15030 | FDA UDI | Class I | Active |
| Curaplex | 8600-01231 | FDA UDI | Class I | Active |
| Curaplex | 19198-0000 | FDA UDI | Class I | Active |
| Curaplex | 444004 | FDA UDI | Class II | Active |
| Curaplex | 661204 | FDA UDI | Class I | Active |
| Curaplex | 1840-01364-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01083 | FDA UDI | Class I | Active |
| Curaplex | 30058 | FDA UDI | Class I | Active |
| Curaplex | 661125 | FDA UDI | Class II | Active |
| Curaplex | 660204 | FDA UDI | Class II | Active |
| Curaplex | 1121-36552 | FDA UDI | Class I | Active |
| Curaplex | S3852P-A | FDA UDI | Class I | Active |
| Curaplex | 2412-001QM | FDA UDI | Class I | Active |
| Curaplex | 8600-01394 | FDA UDI | Class I | Active |
| Curaplex | 8600-SSC06F-1378 | FDA UDI | Class I | Active |
| Curaplex | 68800T | 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 |