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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 9 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | TC3CB-A-HL-ST | FDA UDI | Class I | Active |
| Curaplex | 1612-84130 | FDA UDI | Class II | Active |
| Curaplex | 670135-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01192 | FDA UDI | Class I | Active |
| Curaplex | 12993 | FDA UDI | Class II | Active |
| Curaplex | 16244 | FDA UDI | Class II | Active |
| Curaplex | 8600-VENGRD-1219 | FDA UDI | Class II | Active |
| Curaplex | 5-0236-70 | FDA UDI | Class I | Active |
| Curaplex | BT-B200 | FDA UDI | Class I | Active |
| Curaplex | 2010-34110 | FDA UDI | Class I | Active |
| Curaplex® | 2442-BVMPSA-ET | FDA UDI | Class II | Active |
| Curaplex | 36739 | FDA UDI | Class I | Active |
| Curaplex | 2021-15122 | FDA UDI | Class I | Active |
| Curaplex | 301-170EA | FDA UDI | Class I | Active |
| Curaplex | 16384 | FDA UDI | Class II | Active |
| Curaplex | 1612-84260 | FDA UDI | Class II | Active |
| Curaplex | 8600-SL3MLS-1438 | FDA UDI | Class II | Active |
| Curaplex | 1612-84160 | FDA UDI | Class II | Active |
| Curaplex | 8600-01439 | FDA UDI | Class I | Active |
| Curaplex | 660786 | FDA UDI | Class I | Active |
| Curaplex | 8600-01378 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4685 | FDA UDI | Class I | Active |
| Curaplex | PL545 | FDA UDI | Class I | Active |
| Curaplex | NC102 | FDA UDI | Class I | Active |
| Curaplex | 15327 | FDA UDI | Class I | Active |
| Curaplex | 8600-01496 | FDA UDI | Class II | Active |
| Curaplex | 2113-20285 | FDA UDI | Class II | Active |
| Curaplex | 8600-01297-DOD | FDA UDI | Class II | Active |
| Curaplex | 661139 | FDA UDI | Class I | Active |
| Curaplex | 670221-KIT | FDA UDI | Class I | Active |
| Curaplex | 1841-14003 | FDA UDI | Class I | Active |
| Curaplex | 670166-kit | FDA UDI | Class I | Active |
| Curaplex | 8600-01250 | FDA UDI | Class II | Active |
| Curaplex | 8600-01249 | FDA UDI | Class II | Active |
| Curaplex | 2525-13623 | FDA UDI | Class II | Active |
| Curaplex | AF3000 | FDA UDI | Class II | Active |
| Curaplex | 661469MS | FDA UDI | Class I | Active |
| Curaplex | 533-MS-MED3N | FDA UDI | Class II | Active |
| Curaplex | 8600-01344 | FDA UDI | Class I | Active |
| Curaplex® | 8600-01552 | FDA UDI | Class II | Active |
| Curaplex | 670198-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01233 | FDA UDI | Class I | Active |
| Curaplex | 8600-01457 | FDA UDI | Class I | Active |
| Curaplex | 660116 | FDA UDI | Class II | Active |
| Curaplex | 1071-10210 | FDA UDI | Class I | Active |
| Curaplex | 1216-01106D | FDA UDI | Class I | Active |
| Curaplex | 670013-KIT | FDA UDI | Class II | Active |
| Curaplex | 1860-08708 | FDA UDI | Class II | Active |
| Curaplex | 8600-01491 | FDA UDI | Class I | Active |
| Curaplex | 8600-01511 | 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 |