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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 28 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01354 | FDA UDI | Class II | Active |
| Curaplex | 2525-16050 | FDA UDI | Class II | Active |
| Curaplex | 683924OD | FDA UDI | Class II | Active |
| Curaplex | 8600-STB003A | FDA UDI | Class I | Unknown |
| Curaplex | 2114-16305 | FDA UDI | Class I | Active |
| Curaplex | 563502 | FDA UDI | Class I | Active |
| Curaplex | 8600-01268 | FDA UDI | Class I | Active |
| Curaplex | 2010-34050 | FDA UDI | Class I | Active |
| Curaplex | T100-CASE | FDA UDI | Class III | Active |
| Curaplex | 8600-01420 | FDA UDI | Class II | Active |
| Curaplex | B-3140 | FDA UDI | Class I | Active |
| Curaplex | 661680 | FDA UDI | Class I | Active |
| Curaplex | 1212-12102 | FDA UDI | Class I | Active |
| Curaplex | 670156-KIT | FDA UDI | Class I | Active |
| Curaplex | 2021-15026 | FDA UDI | Class I | Active |
| Curaplex | 36611 | FDA UDI | Class II | Active |
| Curaplex | 14756MS | FDA UDI | Class II | Active |
| Curaplex | 5207F-SE-E | FDA UDI | Class II | Active |
| Curaplex | KLTSD404K-NG | FDA UDI | Class I | Active |
| Curaplex | 661134 | FDA UDI | Class I | Active |
| Curaplex | B5010 | FDA UDI | Class I | Active |
| Curaplex | B-3130 | FDA UDI | Class I | Active |
| Curaplex | B4013 | FDA UDI | Class I | Active |
| Curaplex | 8600-01156 | FDA UDI | Class I | Active |
| Curaplex | 2114-163025 | FDA UDI | Class I | Active |
| Curaplex | 8600-01498 | FDA UDI | Class II | Active |
| Curaplex | B-3100 | FDA UDI | Class I | Active |
| Curaplex | FCBLF-ORG | FDA UDI | Class I | Active |
| Curaplex | 440414 | FDA UDI | Class I | Active |
| Curaplex | 6700139-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01153 | FDA UDI | Class I | Active |
| Curaplex | 2113-20245 | FDA UDI | Class II | Active |
| Curaplex | 8600-01408 | FDA UDI | Class I | Active |
| Curaplex | B-3020 | FDA UDI | Class I | Active |
| Curaplex | 8600-01092 | FDA UDI | Class II | Active |
| Curaplex | 540-1216-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01461 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LT-0 | FDA UDI | Class II | Active |
| Curaplex | 8600-01121 | FDA UDI | Class II | Active |
| Curaplex | 020055 | FDA UDI | Class I | Active |
| Curaplex | 36756 | FDA UDI | Class II | Active |
| Curaplex | 13027 | FDA UDI | Class I | Active |
| Curaplex | 36156 | FDA UDI | Class II | Active |
| Curaplex | 661634 | FDA UDI | Class I | Active |
| Curaplex | 8600-01465 | FDA UDI | Class II | Active |
| Curaplex | 8600-AEMSKP-1486 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MAC-1 | FDA UDI | Class I | Active |
| Curaplex | 1612-84230 | FDA UDI | Class II | Active |
| Curaplex | 8600-01248 | FDA UDI | Class I | Active |
| Curaplex | 18311 | 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 |