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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 38 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 10369 | FDA UDI | Class I | Active |
| Curaplex | G0755-A | FDA UDI | Class II | Active |
| Curaplex | 301-PSC107 | FDA UDI | Class I | Active |
| Curaplex | 8600-IV018G-1214 | FDA UDI | Class II | Active |
| Curaplex | 8600-01171 | FDA UDI | Class II | Active |
| Curaplex | 2525-15022 | FDA UDI | Class II | Active |
| Curaplex | 1206-A | FDA UDI | Class II | Active |
| Curaplex | 301-114 | FDA UDI | Class I | Active |
| Curaplex | 301-PSC11415 | FDA UDI | Class I | Active |
| Curaplex | 290026 | FDA UDI | Class I | Active |
| Curaplex | 2010-35040 | FDA UDI | Class I | Active |
| Curaplex | 8600-01337 | FDA UDI | Class II | Active |
| Curaplex | 8600-01289 | FDA UDI | Class II | Active |
| Curaplex | 1880-93102D-DOD | FDA UDI | Class I | Active |
| Curaplex | 8600-01358 | FDA UDI | Class II | Active |
| Curaplex | 1840-012QM | FDA UDI | Class II | Active |
| Curaplex | 8783 | FDA UDI | Class II | Active |
| Curaplex | XT605-OR-EN | FDA UDI | Class I | Active |
| Curaplex | 670136-KIT | FDA UDI | Class II | Active |
| Curaplex | G0721-A | FDA UDI | Class II | Active |
| Curaplex | 1121-36545 | FDA UDI | Class I | Active |
| Curaplex | 683921 | FDA UDI | Class I | Active |
| Curaplex | 661132 | FDA UDI | Class I | Active |
| Curaplex | 8600-01454 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 028056 | FDA UDI | Class I | Active |
| Curaplex® | SOB1APG-23-KIT | FDA UDI | Class I | Active |
| Curaplex | 1004SP | FDA UDI | Class I | Active |
| Curaplex | 8600-01245 | FDA UDI | Class II | Active |
| Curaplex | 1012-44885 | FDA UDI | Class I | Active |
| Curaplex | 8600-01170 | FDA UDI | Class II | Active |
| Curaplex | 670227-KIT | FDA UDI | Class I | Active |
| Curaplex | 1431-16010 | FDA UDI | Class I | Active |
| Curaplex | 36275 | FDA UDI | Class I | Active |
| Curaplex | 8600-01516 | FDA UDI | Class II | Active |
| Curaplex | 1860-08704 | FDA UDI | Class II | Active |
| Curaplex | 8600-01152 | FDA UDI | Class II | Active |
| Curaplex | 8600-01203 | FDA UDI | Class I | Active |
| Curaplex | 301-189 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-2-S | FDA UDI | Class I | Active |
| Curaplex | 16242 | FDA UDI | Class II | Active |
| Curaplex | 670280-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01352 | FDA UDI | Class II | Active |
| Curaplex | 1507506 | FDA UDI | Class I | Active |
| Curaplex | 1012-47133 | FDA UDI | Class I | Active |
| Curaplex | 1612-84240 | FDA UDI | Class II | Active |
| Curaplex | 677556-2 | FDA UDI | Class II | Active |
| Curaplex | 1212-12104 | FDA UDI | Class I | Active |
| Curaplex | 68496-02P | FDA UDI | Class I | Active |
| Curaplex | 1012-44886 | 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 |