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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 5 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex® | 3271-63402 | FDA UDI | Class I | Active |
| Curaplex® | FGIVBLOOD01-25-KIT | FDA UDI | Class II | Active |
| Curaplex | TA-200DEMOKIT | FDA UDI | Class II | Active |
| Curaplex | 290900L | FDA UDI | Class I | Active |
| Curaplex | 2114-04084-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01397 | FDA UDI | Class I | Active |
| Curaplex | 301-BVM300 | FDA UDI | Class II | Active |
| Curaplex | 8600-01431 | FDA UDI | Class II | Active |
| Curaplex | 670212-KIT | FDA UDI | Class I | Active |
| Curaplex | 36160 | FDA UDI | Class II | Active |
| Curaplex | 670107-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01283 | FDA UDI | Class II | Active |
| Curaplex | 660488 | FDA UDI | Class I | Active |
| Curaplex | 670189-KIT | FDA UDI | Class I | Active |
| Curaplex | B802 | FDA UDI | Class I | Active |
| Curaplex | 29320S | FDA UDI | Class I | Active |
| Curaplex | 2114-16302 | FDA UDI | Class I | Active |
| Curaplex | 36729 | FDA UDI | Class II | Active |
| Curaplex | 2201 | FDA UDI | Class I | Active |
| Curaplex | 681232 | FDA UDI | Class II | Active |
| Curaplex | 8600-01131 | FDA UDI | Class I | Active |
| Curaplex | 12356 | FDA UDI | Class II | Active |
| Curaplex | 670140-KIT | FDA UDI | Class I | Active |
| Curaplex | 670200-KIT | FDA UDI | Class I | Active |
| Curaplex | TC-SMBL2CG1NE0ZABA | FDA UDI | Class I | Active |
| Curaplex | 8600-AEMSKA-1485 | FDA UDI | Class II | Active |
| Curaplex | 670060-KIT | FDA UDI | Class II | Active |
| Curaplex | 681250C | FDA UDI | Class II | Active |
| Curaplex | 2113-10340 | FDA UDI | Class II | Active |
| Curaplex | NSS2003BP | FDA UDI | Class II | Active |
| Curaplex | 14761 | FDA UDI | Class II | Active |
| Curaplex | 1212-12106 | FDA UDI | Class I | Active |
| Curaplex | 1071-10212 | FDA UDI | Class I | Active |
| Curaplex | 16570 | FDA UDI | Class I | Active |
| Curaplex | 8600-NASPED-1595 | FDA UDI | Class I | Active |
| Curaplex | 6872-PRE | FDA UDI | Class II | Active |
| Curaplex | 12186 | FDA UDI | Class II | Active |
| Curaplex | 683925OD | FDA UDI | Class II | Active |
| Curaplex | 8600-01307 | FDA UDI | Class II | Active |
| Curaplex | 2114-193025 | FDA UDI | Class I | Active |
| Curaplex | 670281-KIT | FDA UDI | Class I | Active |
| Curaplex | 36147-2 | FDA UDI | Class II | Active |
| Curaplex | XT605-BL-EN | FDA UDI | Class I | Active |
| Curaplex | 5707F-SE | FDA UDI | Class II | Active |
| Curaplex | 8600-01513 | FDA UDI | Class II | Active |
| Curaplex | 1212-12109 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-YK10EA | FDA UDI | Class II | Active |
| Curaplex | 1071-17367 | FDA UDI | Class I | Active |
| Curaplex | 8600-01434 | FDA UDI | Class I | Active |
| Curaplex | 670186-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 |