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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 27 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2113-20235 | FDA UDI | Class II | Active |
| Curaplex | NSSSTARTB | FDA UDI | Class II | Active |
| Curaplex | 05-00811NEG | FDA UDI | Class II | Active |
| Curaplex | 30079 | FDA UDI | Class II | Active |
| Curaplex | 8600-01468 | FDA UDI | Class II | Active |
| Curaplex | 670105-KIT | FDA UDI | Class II | Active |
| Curaplex | J8023E-A | FDA UDI | Class II | Active |
| Curaplex | 020008C | FDA UDI | Class I | Active |
| Curaplex | 1613-86220 | FDA UDI | Class II | Active |
| Curaplex | 8600-01135 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4665 | FDA UDI | Class I | Active |
| Curaplex | 8600-01313 | FDA UDI | Class II | Active |
| Curaplex | 670019-KIT | FDA UDI | U | Active |
| Curaplex | 1841-14004 | FDA UDI | Class I | Active |
| Curaplex | 1015-47144 | FDA UDI | Class I | Active |
| Curaplex | 13164 | FDA UDI | Class II | Active |
| Curaplex | 30050 | FDA UDI | Class I | Active |
| Curaplex | 8600-01303 | FDA UDI | Class I | Active |
| Curaplex | 8600-01319 | FDA UDI | Class I | Active |
| Curaplex | 8600-01304 | FDA UDI | Class I | Active |
| Curaplex | NALKIT-X2 | FDA UDI | Class II | Active |
| Curaplex | 2113-20250 | FDA UDI | Class II | Active |
| Curaplex | 8600-01327 | FDA UDI | Class II | Active |
| Curaplex | 660424 | FDA UDI | Class II | Active |
| Curaplex | 540-1727EA-A | FDA UDI | Class I | Active |
| Curaplex | 670092-KIT | FDA UDI | Class I | Active |
| Curaplex | 36045 | FDA UDI | Class II | Active |
| Curaplex | 1860-08784 | FDA UDI | Class II | Active |
| Curaplex | 16240 | FDA UDI | Class II | Active |
| Curaplex | 023070S | FDA UDI | Class II | Active |
| Curaplex | 8600-01413 | FDA UDI | Class II | Active |
| Curaplex | 8600-01318 | FDA UDI | Class II | Active |
| Curaplex | P3052EA | FDA UDI | Class II | Active |
| Curaplex | B1110 | FDA UDI | Class I | Active |
| Curaplex | B5130 | FDA UDI | Class I | Active |
| Curaplex | 8600-ATFMLOK | FDA UDI | Class II | Active |
| Curaplex | 1431-16012 | FDA UDI | Class I | Active |
| Curaplex | 670196-KITFBA | FDA UDI | Class I | Active |
| Curaplex | 1121-36569 | FDA UDI | Class I | Active |
| Curaplex | 2113-20325 | FDA UDI | Class II | Active |
| Curaplex | 660788-MB-CAT-DOD | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4630 | FDA UDI | Class I | Active |
| Curaplex | 1612-84120 | FDA UDI | Class II | Active |
| Curaplex | 8600-YANKRS-1379 | FDA UDI | Class II | Active |
| Curaplex | B905 | FDA UDI | Class I | Active |
| Curaplex | 1121-36557 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-010M | FDA UDI | Class I | Active |
| Curaplex | 8600-01265 | FDA UDI | Class II | Active |
| Curaplex | 16107 | FDA UDI | Class II | Active |
| Curaplex | 670058-KIT | 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 |