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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 2 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 73320XL | FDA UDI | Class II | Active |
| Curaplex | 2114-04083-KIT | FDA UDI | Class II | Active |
| Curaplex | AF2000 | FDA UDI | Class II | Active |
| Curaplex | 2745-90080 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-4 | FDA UDI | Class I | Active |
| Curaplex | 2010-35080 | FDA UDI | Class I | Active |
| Curaplex | KLTSD405K-NG | FDA UDI | Class I | Active |
| Curaplex | 680025 | FDA UDI | Class II | Active |
| Curaplex | 8600-01173 | FDA UDI | Class I | Active |
| Curaplex | 8600-01469 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-8122 | FDA UDI | Class I | Active |
| Curaplex | 2021-15124 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-1-M | FDA UDI | Class I | Active |
| Curaplex | 1860-08782 | FDA UDI | Class II | Active |
| Curaplex | 2021-15032 | FDA UDI | Class I | Active |
| Curaplex® | 3271-63400 | FDA UDI | Class I | Active |
| Curaplex | 8600-01272 | FDA UDI | Class I | Active |
| Curaplex | 38012 | FDA UDI | Class II | Active |
| Curaplex | 2-0211-4655 | FDA UDI | Class I | Active |
| Curaplex | 301-0206 | FDA UDI | Class II | Active |
| Curaplex | 8600-01101 | FDA UDI | Class II | Active |
| Curaplex | 8600-01127 | FDA UDI | Class I | Active |
| Curaplex | B-3110 | FDA UDI | Class I | Active |
| Curaplex | 8600-01398 | FDA UDI | Class I | Active |
| Curaplex | 444003 | FDA UDI | Class II | Active |
| Curaplex | 36107 | FDA UDI | Class II | Active |
| Curaplex | 8600-01254 | FDA UDI | Class II | Active |
| Curaplex | 670094-KIT | FDA UDI | Class I | Active |
| Curaplex | 681772K | FDA UDI | Class I | Active |
| Curaplex | 38008 | FDA UDI | Class II | Active |
| Curaplex | KLTSD404K | FDA UDI | Class I | Active |
| Curaplex | 8600-01091 | FDA UDI | Class II | Active |
| Curaplex | 68124SP-S | FDA UDI | Class I | Active |
| Curaplex | 8600-ETTB50-1265 | FDA UDI | Class II | Active |
| Curaplex | 2113-20245 | FDA UDI | Class II | Active |
| Curaplex | 73320M | FDA UDI | Class II | Active |
| Curaplex | 1121-36568 | FDA UDI | Class I | Active |
| Curaplex | 68800S | FDA UDI | Class II | Active |
| Curaplex | 8600-01146 | FDA UDI | Class II | Active |
| Curaplex | 301-44F10-120 | FDA UDI | Class II | Active |
| Curaplex | 301-104 | FDA UDI | Class I | Active |
| Curaplex | 2762-32702 | FDA UDI | Class I | Active |
| Curaplex | 670163-kit | FDA UDI | Class II | Active |
| Curaplex | 38005 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-15 | FDA UDI | Class I | Active |
| Curaplex | 301-44F50-100 | FDA UDI | Class II | Active |
| Curaplex | 1212-12107 | FDA UDI | Class I | Active |
| Curaplex | 2021-15028 | FDA UDI | Class I | Active |
| Curaplex | 670266-KIT | FDA UDI | Class II | Active |
| Curaplex | 021008 | 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 |