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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 6 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 533-MS-YK40EA | FDA UDI | Class II | Active |
| Curaplex | 8600-01378 | FDA UDI | Class I | Active |
| Curaplex | 2010-35100 | FDA UDI | Class I | Active |
| Curaplex | 8600-01302 | FDA UDI | Class I | Active |
| Curaplex | 8600-01440 | FDA UDI | Class II | Active |
| Curaplex | 8600-01416 | FDA UDI | Class I | Active |
| Curaplex | 8600-01396 | FDA UDI | Class I | Active |
| Curaplex | 8600-01278 | FDA UDI | Class II | Active |
| Curaplex | 661964 | FDA UDI | Class II | Active |
| Curaplex | 2021-15036 | FDA UDI | Class I | Active |
| Curaplex | 8600-01232 | FDA UDI | Class I | Active |
| Curaplex | 38011 | FDA UDI | Class II | Active |
| Curaplex | 670170-KIT | FDA UDI | Class II | Active |
| Curaplex | 1340-40000 | FDA UDI | Class I | Active |
| Curaplex | 560503 | FDA UDI | Class I | Active |
| Curaplex | B-3035 | FDA UDI | Class I | Active |
| Curaplex | 351200A | FDA UDI | Class II | Active |
| Curaplex | 660383 | FDA UDI | Class II | Active |
| Curaplex | 670062-KIT | FDA UDI | Class II | Active |
| Curaplex | 1840-26020 | FDA UDI | Class II | Active |
| Curaplex | B2130 | FDA UDI | Class I | Active |
| Curaplex | B4013S | FDA UDI | Class I | Active |
| Curaplex | 301-PSCU10715 | FDA UDI | Class I | Active |
| Curaplex | 2145-13404 | FDA UDI | Class I | Active |
| Curaplex | 680153-KIT | FDA UDI | Class II | Active |
| Curaplex | 10-83611NEG | FDA UDI | Class II | Active |
| Curaplex | 2525-20116 | FDA UDI | Class I | Active |
| Curaplex | 1122-14952 | FDA UDI | Class I | Active |
| Curaplex | 8600-01252 | FDA UDI | Class II | Active |
| Curaplex | 8600-01262 | FDA UDI | Class II | Active |
| Curaplex | 8600-01263 | FDA UDI | Class II | Active |
| Curaplex | 8600-SSC16F-1378 | FDA UDI | Class I | Active |
| Curaplex | 1121-36565 | FDA UDI | Class I | Active |
| Curaplex | 2141-13510 | FDA UDI | Class I | Active |
| Curaplex | 660905 | FDA UDI | Class II | Active |
| Curaplex | 021007 | FDA UDI | Class I | Active |
| Curaplex | 8600-01270 | FDA UDI | Class II | Active |
| Curaplex | 8600-01487 | FDA UDI | Class II | Active |
| Curaplex | 1612-84150 | FDA UDI | Class II | Active |
| Curaplex | B904 | FDA UDI | Class I | Active |
| Curaplex | AF5000 | FDA UDI | Class II | Active |
| Curaplex | B-3120 | FDA UDI | Class I | Active |
| Curaplex | 260414 | FDA UDI | Class I | Active |
| Curaplex | 30078 | FDA UDI | Class II | Active |
| Curaplex | 2113-10280 | FDA UDI | Class II | Active |
| Curaplex | 1980 | FDA UDI | Class I | Active |
| Curaplex | 1212-12113 | FDA UDI | Class I | Active |
| Curaplex | 8600-01294 | FDA UDI | Class II | Active |
| Curaplex | 8600-01217 | FDA UDI | Class II | Active |
| Curaplex | 670134-KIT | FDA UDI | Class II | Active |
Related Companies
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Authorities
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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 |