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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 39 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | B5120 | FDA UDI | Class I | Active |
| Curaplex | 8600-01304 | FDA UDI | Class I | Active |
| Curaplex | 2113-20275 | FDA UDI | Class II | Active |
| Curaplex | 670214-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01390 | FDA UDI | Class II | Active |
| Curaplex | 2113-20230 | FDA UDI | Class II | Active |
| Curaplex | 3245-19123 | FDA UDI | Class I | Active |
| Curaplex | B902 | FDA UDI | Class I | Active |
| Curaplex | 660448-VENT | FDA UDI | Class I | Active |
| Curaplex | B5030 | FDA UDI | Class I | Active |
| Curaplex | 8600-01198 | FDA UDI | Class II | Active |
| Curaplex | NC101 | FDA UDI | Class I | Active |
| Curaplex | TC1B-I-CP-ST | FDA UDI | Class II | Active |
| Curaplex | ATFSABTK | FDA UDI | Class I | Active |
| Curaplex | 36093 | FDA UDI | Class II | Active |
| Curaplex | 8600-01385 | FDA UDI | Class I | Active |
| Curaplex | J8023V | FDA UDI | Class II | Active |
| Curaplex | 1015-47145 | FDA UDI | Class I | Active |
| Curaplex | 2525-01094 | FDA UDI | Class II | Active |
| Curaplex® | 8600-01521 | FDA UDI | Class II | Active |
| Curaplex | 12995 | FDA UDI | Class II | Active |
| Curaplex | 670016-KIT | FDA UDI | U | Active |
| Curaplex | 8600-BLOODDRAW-CS | FDA UDI | Class II | Active |
| Curaplex | 1012-44886 | FDA UDI | Class I | Active |
| Curaplex | 8600-01417 | FDA UDI | Class I | Active |
| Curaplex | 8600-01276 | FDA UDI | Class II | Active |
| Curaplex | 540-1330EA-A | FDA UDI | Class II | Active |
| Curaplex | BT-40520 | FDA UDI | Class I | Active |
| Curaplex | 2741-50486 | FDA UDI | Class II | Active |
| Curaplex | 2145-13500 | FDA UDI | Class I | Active |
| Curaplex | 8600-EKGLAD-1329 | FDA UDI | Class II | Active |
| Curaplex | 670003-KIT | FDA UDI | Class I | Active |
| Curaplex | 1212-12101 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-010S | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | SIVSTTCHP-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 1340-27000 | FDA UDI | Class I | Active |
| Curaplex | 8600-01316 | FDA UDI | Class II | Active |
| Curaplex | TC-DLCB2CG1A1GBBT | FDA UDI | Class I | Active |
| Curaplex | 670282-KIT | FDA UDI | Class I | Active |
| Curaplex | 1212-12106 | FDA UDI | Class I | Active |
| Curaplex | 680150-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01113 | FDA UDI | Class II | Active |
| Curaplex | TC2B-B-ML-ST | FDA UDI | Class I | Active |
| Curaplex | 8600-01334 | FDA UDI | Class I | Active |
| Curaplex | 1841-14010 | FDA UDI | Class I | Active |
| Curaplex | 2113-10265 | FDA UDI | Class II | Active |
| Curaplex | 680125-KIT | FDA UDI | Class I | Active |
| Curaplex | 1071-10202 | FDA UDI | Class I | Active |
| Curaplex | 1012-44983 | 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 |