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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 19 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-EPIKITRP | FDA UDI | Class I | Active |
| Curaplex | 8600-01293 | FDA UDI | Class II | Active |
| Curaplex | 2113-10225 | FDA UDI | Class II | Active |
| Curaplex | 2-0211-4660 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2113-20320 | FDA UDI | Class II | Active |
| Curaplex | 1012-44883 | FDA UDI | Class I | Active |
| Curaplex | 8600-01163 | FDA UDI | Class I | Active |
| Curaplex | 540-1721EA-A | FDA UDI | Class I | Active |
| Curaplex | 1212-12102 | FDA UDI | Class I | Active |
| Curaplex | 8600-01230 | FDA UDI | Class II | Active |
| Curaplex | 1880-93102D | FDA UDI | Class I | Active |
| Curaplex | 1431-77000 | FDA UDI | Class I | Active |
| Curaplex | 2114-19305 | FDA UDI | Class I | Active |
| Curaplex | 8600-01145 | FDA UDI | Class I | Active |
| Curaplex | 670143-KIT-DOD | FDA UDI | Class II | Active |
| Curaplex | 8600-01343 | FDA UDI | Class I | Active |
| Curaplex | 2021-15012 | FDA UDI | Class I | Active |
| Curaplex | 777557-1 | FDA UDI | Class II | Active |
| Curaplex | 8600-01388 | FDA UDI | Class II | Active |
| Curaplex | 30070 | FDA UDI | Class II | Active |
| Curaplex | 301-PASC107 | FDA UDI | Class I | Active |
| Curaplex | 8600-01210 | FDA UDI | Class II | Active |
| Curaplex | 8600-01260 | FDA UDI | Class I | Active |
| Curaplex | 8600-G0025 | FDA UDI | Class II | Active |
| Curaplex | 8600-01314 | FDA UDI | Class II | Active |
| Curaplex | 661420-B | FDA UDI | Class II | Active |
| Curaplex | 8600-01300 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-4 | FDA UDI | Class I | Active |
| Curaplex | 1613-86224 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-1-M | FDA UDI | Class I | Active |
| Curaplex | EMP3250GC | FDA UDI | Class I | Active |
| Curaplex | 60-83011NEG | FDA UDI | Class II | Active |
| Curaplex | 30056 | FDA UDI | Class I | Active |
| Curaplex | 382000RC | FDA UDI | Class I | Active |
| Medstorm Defibrillator Pad | T100-CS | FDA UDI | Class III | Unknown |
| Curaplex | 2112-38004 | FDA UDI | Class II | Active |
| Curaplex | 2114-19303 | FDA UDI | Class I | Active |
| Curaplex | 13301 | FDA UDI | Class II | Active |
| Curaplex | 3020-28013 | FDA UDI | Class I | Active |
| Curaplex | 1715-01827 | FDA UDI | Class II | Active |
| Curaplex | BLS-8700KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01126 | FDA UDI | Class II | Active |
| Curaplex | 560502 | FDA UDI | Class I | Active |
| Curaplex | 355-3222-EEA | FDA UDI | Class I | Active |
| Curaplex | 8600-01324 | FDA UDI | Class I | Active |
| Curaplex | 670242-KIT | FDA UDI | Class II | Active |
| Curaplex | 1121-36551 | FDA UDI | Class I | Active |
| Curaplex | 670231-KIT | FDA UDI | Class II | Active |
| Curaplex | 38007 | 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 |