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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 33 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1121-36550 | FDA UDI | Class I | Active |
| Curaplex | 8600-SFMINF-1593 | FDA UDI | Class I | Active |
| Curaplex | 1012-44985 | FDA UDI | Class I | Active |
| Curaplex | 38021 | FDA UDI | Class II | Active |
| Curaplex | KLTSD403K-NG | FDA UDI | Class I | Active |
| Curaplex | 670263-KIT | FDA UDI | Class I | Active |
| Curaplex | B5020 | FDA UDI | Class I | Active |
| Curaplex | 2811-05532 | FDA UDI | Class I | Active |
| Curaplex | 14043 | FDA UDI | Class I | Active |
| Curaplex | 661137 | FDA UDI | Class I | Active |
| Curaplex | 8600-01453 | FDA UDI | Class II | Active |
| Curaplex | 8600-01448 | FDA UDI | Class II | Active |
| Curaplex | 301-160EA | FDA UDI | Class I | Active |
| Curaplex | 38016 | FDA UDI | Class II | Active |
| Curaplex | KLTSD404K-DOD | FDA UDI | Class I | Active |
| Curaplex | 2811-05524 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-103S | FDA UDI | Class I | Active |
| Curaplex | 2010-35060 | FDA UDI | Class I | Active |
| Curaplex | 2145-13504 | FDA UDI | Class I | Active |
| Curaplex | TC2CB-A-ML-ST | FDA UDI | Class I | Active |
| Curaplex | 1122-14958 | FDA UDI | Class I | Active |
| Curaplex | 36164 | FDA UDI | Class II | Active |
| Curaplex | STB002I-XT | FDA UDI | Class I | Active |
| Curaplex | B2120 | FDA UDI | Class I | Active |
| Curaplex | 36022 | FDA UDI | Class I | Active |
| Curaplex | TC-MMBL2CG4A1ZBBA | FDA UDI | Class I | Active |
| Curaplex | 8600-0INTS0-1218 | FDA UDI | Class II | Active |
| Curaplex | 477-KLTSD412 | FDA UDI | Class I | Active |
| Curaplex | 8600-01285 | FDA UDI | Class II | Active |
| Curaplex | 68142-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01301 | FDA UDI | Class II | Active |
| Curaplex | 351202-A | FDA UDI | Class II | Active |
| Curaplex | 1840-01339-A | FDA UDI | Class II | Active |
| Curaplex | 670173-kit | FDA UDI | Class II | Active |
| Curaplex | SEEPEDNA | FDA UDI | Class I | Active |
| Curaplex | 8600-01086 | FDA UDI | Class II | Active |
| Curaplex | 1212-12101 | FDA UDI | Class I | Active |
| Curaplex | 8600-01286 | FDA UDI | Class I | Active |
| Curaplex | 8600-01509 | FDA UDI | Class II | Active |
| Curaplex | 660347 | FDA UDI | Class II | Active |
| Curaplex | 2113-10330 | FDA UDI | Class II | Active |
| Curaplex | 8600-01372 | FDA UDI | Class I | Active |
| Curaplex | 1840-014QM | FDA UDI | Class II | Active |
| Curaplex | 660787 | FDA UDI | Class I | Active |
| Curaplex | 1860-08786 | FDA UDI | Class II | Active |
| Curaplex | 36150 | FDA UDI | Class II | Active |
| Curaplex | TC3B-B-HL-ST | FDA UDI | Class I | Active |
| Curaplex | 69100MS | FDA UDI | Class II | Active |
| Curaplex | 670157-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01297 | 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 |