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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 8 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 301-FO-WH-2 | FDA UDI | Class I | Active |
| Curaplex | 8600-01411 | FDA UDI | Class I | Active |
| Curaplex | 680155-KIT | FDA UDI | Class II | Active |
| Curaplex | 14651 | FDA UDI | Class II | Active |
| Curaplex | CUR5602 | FDA UDI | Class I | Active |
| Curaplex | 2525-19341 | FDA UDI | Class I | Active |
| Curaplex | 36106 | FDA UDI | Class II | Active |
| Curaplex | 8600-01409 | FDA UDI | Class II | Active |
| Curaplex | 2114-16305 | FDA UDI | Class I | Active |
| Curaplex | 2010-35050 | FDA UDI | Class I | Active |
| Curaplex | 2114-163025 | FDA UDI | Class I | Active |
| Curaplex | 12317 | FDA UDI | Class II | Active |
| Curaplex | 8600-01276 | FDA UDI | Class II | Active |
| Curaplex | 670126-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01123 | FDA UDI | Class II | Active |
| Curaplex | 1979 | FDA UDI | Class I | Active |
| Curaplex | 678007 | FDA UDI | Class II | Active |
| Curaplex | 670165 | FDA UDI | Class II | Active |
| Curaplex | 3246-12345 | FDA UDI | Class I | Active |
| Curaplex | 8600-01281 | FDA UDI | Class II | Active |
| Curaplex | 301-8600-01264 | FDA UDI | Class II | Active |
| Curaplex | 670262-KIT | FDA UDI | Class I | Active |
| Curaplex | 1860-08710 | FDA UDI | Class II | Active |
| Curaplex | 36014 | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | SFA25P-23-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-3 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-00 | FDA UDI | Class I | Active |
| Curaplex | 301-PSCU11415 | FDA UDI | Class I | Active |
| Curaplex® | 8600-01517 | FDA UDI | Class I | Active |
| Curaplex® | 1015-47155 | FDA UDI | Class I | Active |
| Curaplex | 36012 | FDA UDI | Class II | Active |
| Curaplex | 1712-58031 | FDA UDI | Class II | Active |
| Curaplex | 8600-01444 | FDA UDI | Class II | Active |
| Curaplex | B4014 | FDA UDI | Class I | Active |
| Curaplex | 670276-KIT | FDA UDI | Class I | Active |
| Curaplex | 2115-01975 | FDA UDI | Class II | Active |
| Curaplex | 477-KLTSD4125 | FDA UDI | Class I | Active |
| Curaplex | 670067-KIT | FDA UDI | Class II | Active |
| Curaplex | 2114-14004 | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2113-10285 | FDA UDI | Class II | Active |
| Curaplex | 670193-KIT | FDA UDI | Class I | Active |
| Curaplex | 36157 | FDA UDI | Class II | Active |
| Curaplex | B901 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-M | FDA UDI | Class I | Active |
| Curaplex | 2114-193015 | FDA UDI | Class I | Active |
| Curaplex | MS-42210 | FDA UDI | Class I | Active |
| Curaplex | 36105 | FDA UDI | Class II | Active |
| Curaplex | 2114-19304 | 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 |