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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 23 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2113-20265 | FDA UDI | Class II | Active |
| Curaplex | EMP3245N | FDA UDI | Class II | Active |
| Curaplex | 36186 | FDA UDI | Class II | Active |
| Curaplex | 8600-01172 | FDA UDI | Class II | Active |
| Curaplex | 301-115 | FDA UDI | Class I | Active |
| Curaplex | 2113-20320 | FDA UDI | Class II | Active |
| Curaplex | 8600-01363 | FDA UDI | Class II | Active |
| Curaplex | 1712-00361 | FDA UDI | Class II | Active |
| Curaplex | 660788-CAT | FDA UDI | Class I | Active |
| Curaplex | 441260 | FDA UDI | Class I | Active |
| Curaplex | 8600-01325 | FDA UDI | Class I | Active |
| Curaplex® | 1015-47152 | FDA UDI | Class I | Active |
| Curaplex | STB001B-AMAZON | FDA UDI | Class I | Active |
| Curaplex | 36023 | FDA UDI | Class I | Active |
| Curaplex | 73320M | FDA UDI | Class II | Active |
| Curaplex | B1000 | FDA UDI | Class I | Active |
| Curaplex | 8600-01253 | FDA UDI | Class II | Active |
| Curaplex | 660788-MB | FDA UDI | Class I | Active |
| Curaplex | 2114-16302 | FDA UDI | Class I | Active |
| Curaplex | 670014-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01370 | FDA UDI | Class III | Active |
| Curaplex | 670004-KIT | FDA UDI | Class II | Active |
| Curaplex | 2021-15016 | FDA UDI | Class I | Active |
| Curaplex | 8600-01273 | FDA UDI | Class I | Active |
| Curaplex | 670039-KIT | FDA UDI | Class I | Active |
| Curaplex | 30070 | FDA UDI | Class II | Active |
| Curaplex | 8600-01495 | FDA UDI | Class I | Active |
| Curaplex | 1330-85300 | FDA UDI | U | Active |
| Curaplex | 670145-KIT | FDA UDI | Class II | Active |
| Curaplex | 2114-19304 | FDA UDI | Class I | Active |
| Curaplex | 36102 | FDA UDI | Class II | Active |
| Curaplex | 670011-KIT | FDA UDI | Class I | Active |
| Curaplex | 5810 | FDA UDI | Class I | Active |
| Curaplex | 301-144EA | FDA UDI | Class I | Active |
| Curaplex | 686505R | FDA UDI | Class II | Active |
| Curaplex | 670068-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01375 | FDA UDI | Class I | Active |
| Curaplex | B4012 | FDA UDI | Class I | Active |
| Curaplex | 8600-01201 | FDA UDI | Class I | Active |
| Curaplex | TC3B-I-HL-ST | FDA UDI | Class I | Active |
| Curaplex | 8600-01244 | FDA UDI | Class I | Active |
| Curaplex | 36152 | FDA UDI | Class II | Active |
| Curaplex | 670159-kit | FDA UDI | Class I | Active |
| Curaplex | 660200 | FDA UDI | Class II | Active |
| Curaplex | 2113-10240 | FDA UDI | Class II | Active |
| Curaplex | 670139-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-1-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01381 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-3 | FDA UDI | Class I | Active |
| Curaplex | 670243-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 |