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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 36 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 301-BVM1000 | FDA UDI | Class II | Active |
| Curaplex | 8600-01382 | FDA UDI | Class I | Active |
| Curaplex | 301-122EA | FDA UDI | Class I | Active |
| Curaplex | SIVSTTCF-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 660788 | FDA UDI | Class I | Active |
| Curaplex | 301-189U | FDA UDI | Class I | Active |
| Curaplex | 301-LED-WH1-S | FDA UDI | Class I | Active |
| Curaplex | 301-LED-000M | FDA UDI | Class I | Active |
| Curaplex | 8600-01422 | FDA UDI | Class II | Active |
| Curaplex | 36167 | FDA UDI | Class II | Active |
| Curaplex | 30057 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 670211-KIT | FDA UDI | Class II | Active |
| Curaplex | 36020 | FDA UDI | Class I | Active |
| Curaplex® | SCPAPMD301-24-KIT | FDA UDI | Class II | Active |
| Curaplex | SEEGAK | FDA UDI | Class I | Active |
| Curaplex | 1122-14954 | FDA UDI | Class I | Active |
| Curaplex | 2113-10330 | FDA UDI | Class II | Active |
| Curaplex | 670240-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01306 | FDA UDI | Class I | Active |
| Curaplex | 670088-KIT | FDA UDI | Class II | Active |
| Curaplex | 73320XXX | FDA UDI | Class II | Active |
| Curaplex | 8600-01211 | FDA UDI | Class II | Active |
| Curaplex | 8600-01430 | FDA UDI | Class II | Active |
| Curaplex | 301-P3054 | FDA UDI | Class II | Active |
| Curaplex | 1840-92306 | FDA UDI | Class I | Active |
| Curaplex | 301-100EA | FDA UDI | Class I | Active |
| Curaplex | 684267C | FDA UDI | Class II | Active |
| Curaplex | STB001B-XT | FDA UDI | Class I | Active |
| Curaplex | 660787-MB | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2021-15018 | FDA UDI | Class I | Active |
| Curaplex | 8600-01348 | FDA UDI | Class II | Active |
| Curaplex | 8600-01333 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-040S | FDA UDI | Class I | Active |
| Curaplex | 301-LED-PH1-S | FDA UDI | Class I | Active |
| Curaplex | 1212-12112 | FDA UDI | Class I | Active |
| Curaplex | 670082-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-670255-KIT | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4640 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LTEZ | FDA UDI | Class II | Active |
| Curaplex | 301-145EA | FDA UDI | Class I | Active |
| Curaplex | 670097-KIT | FDA UDI | Class II | Active |
| Curaplex | 64250 | FDA UDI | Class II | Active |
| Curaplex | 1840-010QM | FDA UDI | Class II | Active |
| Curaplex | 8600-01356 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-S | FDA UDI | Class I | Active |
| Curaplex | TA-UEP | FDA UDI | Class II | Active |
| Curaplex | 020036 | FDA UDI | Class I | Active |
| Curaplex | 670037-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 |