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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 14 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1212-12114 | FDA UDI | Class I | Active |
| Curaplex | 1012-47135 | FDA UDI | Class I | Active |
| Curaplex | 1712-00360 | FDA UDI | Class II | Active |
| Curaplex | 2113-10250 | FDA UDI | Class II | Active |
| Curaplex | 2113-10330 | FDA UDI | Class II | Active |
| Curaplex | 670170-KIT-DOD | FDA UDI | Class II | Active |
| Curaplex | 670174-KIT | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 670260-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-LED-1015M | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 1212-12111 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-8126 | FDA UDI | Class I | Active |
| Curaplex | 6700138-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-181EA | FDA UDI | Class I | Active |
| Curaplex | 686505B | FDA UDI | Class II | Active |
| Curaplex | 36166 | FDA UDI | Class II | Active |
| Curaplex | 1841-14006 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-25060EA | FDA UDI | Class I | Active |
| Curaplex | 32499MHQ2015 | FDA UDI | Class I | Active |
| Curaplex | 8600-01471 | FDA UDI | Class II | Active |
| Curaplex | 5107ET | FDA UDI | Class II | Active |
| Curaplex | B2140 | FDA UDI | Class I | Active |
| Curaplex | B5150 | FDA UDI | Class I | Active |
| Curaplex | 2115-23128 | FDA UDI | Class I | Active |
| Curaplex | 301-181EA | FDA UDI | Class I | Active |
| Curaplex | 382000BC | FDA UDI | Class II | Active |
| Curaplex | EMP3250GCO | FDA UDI | Class II | Active |
| Curaplex | 8600-01119 | FDA UDI | Class II | Active |
| Curaplex | 2113-20260 | FDA UDI | Class II | Active |
| Curaplex | 36621 | FDA UDI | U | Active |
| Curaplex | 477-KLTSD411 | FDA UDI | Class I | Active |
| Curaplex | 507650 | FDA UDI | Class I | Active |
| Curaplex | 670069-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01464 | FDA UDI | Class II | Active |
| Curaplex | 8600-01387 | FDA UDI | Class I | Active |
| Curaplex | 8600-01450 | FDA UDI | Class I | Active |
| Curaplex | TC-MMBL2CG1A0GBBH | FDA UDI | Class I | Active |
| Curaplex | 533-MS-YK30EA | FDA UDI | Class II | Active |
| Curaplex | 1071-17367 | FDA UDI | Class I | Active |
| Curaplex | 670206-KIT | FDA UDI | Class I | Active |
| Curaplex | 351632I-A | FDA UDI | Class II | Active |
| Curaplex | SEEPNEK | FDA UDI | Class II | Active |
| Curaplex | 8600-01393 | FDA UDI | Class I | Active |
| Curaplex | 1012-44885 | FDA UDI | Class I | Active |
| Curaplex | 5-0236-10 | FDA UDI | Class I | Active |
| Curaplex | 2430-26856 | FDA UDI | Class II | Active |
| Curaplex | 8600-01500 | FDA UDI | Class II | Active |
| Curaplex | 2114-19302 | FDA UDI | Class I | Active |
| Curaplex | 660448-QC | 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 |