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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
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020460367
- DUNS Number
- —
Catalogue (2165)
Page 25 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01384 | FDA UDI | Class I | Active |
| Curaplex | 36619 | FDA UDI | Class I | Active |
| Curaplex | 680156-KIT | FDA UDI | Class II | Active |
| Curaplex | 36095 | FDA UDI | Class II | Active |
| Curaplex | 60-83011 | FDA UDI | Class II | Active |
| Curaplex | 670192-KIT | FDA UDI | Class I | Active |
| Curaplex | 533-MS-002PMP | FDA UDI | Class I | Active |
| Curaplex | 1212-12100 | FDA UDI | Class I | Active |
| Curaplex | 2021-15014 | FDA UDI | Class I | Active |
| Curaplex | 1121-36571 | FDA UDI | Class I | Active |
| Curaplex® | 2442-BVMPIC | FDA UDI | Class II | Active |
| Curaplex | 14762MS | FDA UDI | Class II | Active |
| Curaplex | TC1B-I-CP-CAT | FDA UDI | Class II | Active |
| Curaplex | 2113-10235 | FDA UDI | Class II | Active |
| Curaplex | 1978 | FDA UDI | Class I | Active |
| Curaplex | SFA50PB-23-KIT | FDA UDI | Class I | Active |
| Curaplex | 661136 | FDA UDI | Class I | Active |
| Curaplex | 16602 | FDA UDI | Class I | Active |
| Curaplex | 301-101EA | FDA UDI | Class I | Active |
| Curaplex | 301-112EA | FDA UDI | Class I | Active |
| Curaplex | 14757MS | FDA UDI | Class II | Active |
| Curaplex | 2113-10230 | FDA UDI | Class II | Active |
| Curaplex | 30052 | FDA UDI | Class I | Active |
| Curaplex | 8600-STB002I | FDA UDI | Class I | Active |
| Curaplex | 1212-12108 | FDA UDI | Class I | Active |
| Curaplex | 2114-15005 | FDA UDI | Class II | Active |
| Curaplex | 8600-01383 | FDA UDI | Class I | Active |
| Curaplex | 2114-16304 | FDA UDI | Class I | Active |
| Curaplex | 670029-KIT | FDA UDI | Class II | Active |
| Curaplex | 2430-26855 | FDA UDI | Class II | Active |
| Curaplex | 670187-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01359 | FDA UDI | Class II | Active |
| Curaplex | 8600-01437 | FDA UDI | Class II | Active |
| Curaplex | 670196-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-BVM1500 | FDA UDI | Class II | Active |
| Curaplex | 8600-01312 | FDA UDI | Class II | Active |
| Curaplex | 8600-01317 | FDA UDI | Class II | Active |
| Curaplex | B1240 | FDA UDI | Class I | Active |
| Curaplex | 1215-22195 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-1-S | FDA UDI | Class I | Active |
| Curaplex | B2050 | FDA UDI | Class I | Active |
| Curaplex | 670145-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01165 | FDA UDI | Class II | Active |
| Curaplex® | 1015-47162 | FDA UDI | Class I | Active |
| Curaplex | B906 | FDA UDI | Class I | Active |
| Curaplex | 020008 | FDA UDI | Class I | Active |
| Curaplex | 1012-47140 | FDA UDI | Class I | Active |
| Curaplex | 8600-01243 | FDA UDI | Class I | Active |
| Curaplex | 670247-KIT | FDA UDI | Class II | Active |
| Curaplex | 290900 | 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 |