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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 40 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2010-37110 | FDA UDI | Class I | Active |
| Curaplex | 670040-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01369 | FDA UDI | Class I | Active |
| Curaplex | TC3CB-B-HL-ST | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-00-S | FDA UDI | Class I | Active |
| Curaplex | 680122-KIT | FDA UDI | Class I | Active |
| Curaplex | TC2B-I-ML-CAT | FDA UDI | Class I | Active |
| Curaplex | 14757MS | FDA UDI | Class II | Active |
| Curaplex | B850 | FDA UDI | Class I | Active |
| Curaplex | 5-0236-69 | FDA UDI | Class I | Active |
| Curaplex | 301-191 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-PH2-S | FDA UDI | Class I | Active |
| Curaplex | 2010-34060 | FDA UDI | Class I | Active |
| Curaplex | 2145-13401 | FDA UDI | Class I | Active |
| Curaplex | 682010 | FDA UDI | Class I | Active |
| Curaplex | 301-180EA | FDA UDI | Class I | Active |
| Curaplex | TC1B-B-CP-CAT | FDA UDI | Class II | Active |
| Curaplex | 1012-44884 | FDA UDI | Class I | Active |
| Curaplex | 301-0317D | FDA UDI | Class II | Active |
| Curaplex | 8600-01277 | FDA UDI | Class II | Active |
| Curaplex | 680503 | FDA UDI | Class I | Active |
| Curaplex | TC3B-B-HL-CAT | FDA UDI | Class I | Active |
| Curaplex | 301-120EA | FDA UDI | Class I | Active |
| Curaplex | 8600-01106 | FDA UDI | Class II | Active |
| Curaplex | 660532 | FDA UDI | Class II | Active |
| Curaplex | 8600-01280 | FDA UDI | Class II | Active |
| Curaplex | 2010-35110 | FDA UDI | Class I | Active |
| Curaplex | 8600-01320 | FDA UDI | Class II | Active |
| Curaplex | 2021-15034 | FDA UDI | Class I | Active |
| Curaplex | 36103 | FDA UDI | Class I | Active |
| Curaplex | 670226-KIT | FDA UDI | Class II | Active |
| Curaplex | 1507506 | FDA UDI | Class I | Active |
| Curaplex | 36021 | FDA UDI | Class I | Active |
| Curaplex | 670277-KIT | FDA UDI | Class I | Active |
| Curaplex | B5140 | FDA UDI | Class I | Active |
| Curaplex | 670204-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-117 | FDA UDI | Class I | Active |
| Curaplex | 8600-01158 | FDA UDI | Class II | Active |
| Curaplex | 8600-01482 | FDA UDI | Class I | Active |
| Curaplex | 1121-36561 | FDA UDI | Class I | Active |
| Curaplex | 2113-10290 | FDA UDI | Class II | Active |
| Curaplex | 1612-84160 | FDA UDI | Class II | Active |
| Curaplex | 670131-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-LED-WH1-M | FDA UDI | Class I | Active |
| Curaplex | 8600-01196 | FDA UDI | Class I | Active |
| Curaplex | 8600-01452 | FDA UDI | Class I | Active |
| Curaplex | 1613-86222 | FDA UDI | Class II | Active |
| Curaplex | 670258-KIT | FDA UDI | Class II | Active |
| Curaplex | 2811-05525 | FDA UDI | Class I | Active |
| Curaplex | 1431-55000 | 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 |