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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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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020460367
- DUNS Number
- —
Catalogue (2165)
Page 44 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 301-FO-WH-1 | FDA UDI | Class I | Active |
| Curaplex | 8600-01505 | FDA UDI | Class I | Active |
| Curaplex | B852 | FDA UDI | Class I | Active |
| Curaplex | 5714F-SE-E | FDA UDI | Class II | Active |
| Curaplex | 8600-01386 | FDA UDI | Class I | Active |
| Curaplex | 1212-12103 | FDA UDI | Class I | Active |
| Curaplex | 301-0317C | FDA UDI | Class II | Active |
| Curaplex | 4440010-B | FDA UDI | Class II | Active |
| Curaplex | 8600-ETTB85-1272 | FDA UDI | Class II | Active |
| Curaplex® | 1015-47164 | FDA UDI | Class I | Active |
| Curaplex | 290900XX | FDA UDI | Class I | Active |
| Curaplex | 8600-01425 | FDA UDI | Class II | Active |
| Curaplex | 2021-15116 | FDA UDI | Class I | Active |
| Curaplex | 1012-44883 | FDA UDI | Class I | Active |
| Curaplex | 662309 | 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 |