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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 26 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01374 | FDA UDI | Class I | Active |
| Curaplex | 8600-01213 | FDA UDI | Class I | Active |
| Curaplex | 670239-KIT | FDA UDI | Class II | Active |
| Curaplex | 36797 | FDA UDI | Class II | Active |
| Curaplex | SEENEBK | FDA UDI | Class II | Active |
| Curaplex | 2021-15022 | FDA UDI | Class I | Active |
| Curaplex | 14758MS | FDA UDI | Class II | Active |
| Curaplex | H0335 | FDA UDI | Class II | Active |
| Curaplex | 8600-01329 | FDA UDI | Class I | Active |
| Curaplex® | 8600-01551 | FDA UDI | Class II | Active |
| Curaplex | 2113-10285 | FDA UDI | Class II | Active |
| Curaplex | 30557 | FDA UDI | Class II | Active |
| Curaplex | SEEBAK-BX | FDA UDI | Class I | Active |
| Curaplex | 651776 | FDA UDI | Class II | Active |
| Curaplex | 38010 | FDA UDI | Class II | Active |
| Curaplex | 2113-10335 | FDA UDI | Class II | Active |
| Curaplex | TC1CB-B-CP-ST | FDA UDI | Class II | Active |
| Curaplex | 36011 | FDA UDI | Class II | Active |
| Curaplex | 8600-01186UP | FDA UDI | Class I | Active |
| Curaplex | TA-SEP | FDA UDI | Class II | Active |
| Curaplex | 8600-01193 | FDA UDI | Class I | Active |
| Curaplex | 1840-013QM | FDA UDI | Class II | Active |
| Curaplex | 2145-13403 | FDA UDI | Class I | Active |
| Curaplex | NSSBISH | FDA UDI | Class II | Active |
| Curaplex | 660925 | FDA UDI | Class I | Active |
| Curaplex | 8600-01233 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 1840-20142 | FDA UDI | Class II | Active |
| Curaplex | 670020-KIT | FDA UDI | Class I | Active |
| Curaplex | SEEFRKIT-TQ | FDA UDI | Class I | Active |
| Curaplex | 680152-KIT | FDA UDI | Class I | Active |
| Curaplex | 1715-01837-DOD | FDA UDI | Class II | Active |
| Curaplex | SFA50PA-23-KIT | FDA UDI | Class I | Active |
| Curaplex | B4022 | FDA UDI | Class I | Active |
| Curaplex | 36610 | FDA UDI | Class II | Active |
| Curaplex | 670199-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-FO-PH-1 | FDA UDI | Class I | Active |
| Curaplex | KLTSD405K | FDA UDI | Class I | Active |
| Curaplex | 670256-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01401 | FDA UDI | Class II | Active |
| Curaplex | 8600-01234 | FDA UDI | Class II | Active |
| Curaplex | 1840-32309-A | FDA UDI | Class II | Active |
| Curaplex | 670235-KIT | FDA UDI | Class II | Active |
| Curaplex | 5114F-SE | FDA UDI | Class II | Active |
| Curaplex | 2021-15134 | FDA UDI | Class I | Active |
| Curaplex | 301-5807F-SE | FDA UDI | Class II | Active |
| Curaplex | 533-MS-MED5O | FDA UDI | Class II | Active |
| Curaplex | 8600-IV020G-1215 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-WH15-S | FDA UDI | Class I | Active |
| Curaplex | 2021-15118 | FDA UDI | Class I | Active |
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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 |