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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 21 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2160-20500 | FDA UDI | Class II | Active |
| Curaplex | 30053 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LTEZ-MSA | FDA UDI | Class II | Active |
| Curaplex | 301-107EA | FDA UDI | Class I | Active |
| Curaplex | 301-FO-PH2-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01403 | FDA UDI | Class II | Active |
| Curaplex® | SCPAPMD302-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01402 | FDA UDI | Class II | Active |
| Curaplex | 36155 | FDA UDI | Class II | Active |
| Curaplex | 14756MS | FDA UDI | Class II | Active |
| Curaplex | 8600-01412 | FDA UDI | Class I | Active |
| Curaplex | 660223-DOS | FDA UDI | Class I | Active |
| Curaplex | 8600-01442 | FDA UDI | Class II | Active |
| Curaplex | 8600-01400 | FDA UDI | Class II | Active |
| Curaplex | TC2CB-I-ML-ST | FDA UDI | Class I | Active |
| Curaplex | 73320XXXX | FDA UDI | Class II | Active |
| Curaplex | 686011-A | FDA UDI | Class I | Active |
| Curaplex | 5707F-SE-E | FDA UDI | Class II | Active |
| Curaplex | 95002 | FDA UDI | Class I | Active |
| Curaplex | B4021 | FDA UDI | Class I | Active |
| Curaplex | 8600-STB001B | FDA UDI | Class I | Unknown |
| Curaplex | 502100P | FDA UDI | Class I | Active |
| Curaplex | 8600-01279 | FDA UDI | Class II | Active |
| Curaplex | 8600-01335 | FDA UDI | Class I | Active |
| Curaplex | B1035 | FDA UDI | Class I | Active |
| Curaplex | TC2CB-I-ML-CAT | FDA UDI | Class I | Active |
| Curaplex | 8600-01429 | FDA UDI | Class II | Active |
| Curaplex | 2021-15120 | FDA UDI | Class I | Active |
| Curaplex | 36163 | FDA UDI | Class II | Active |
| Curaplex | 36025 | FDA UDI | Class I | Active |
| Curaplex | 1612-84245 | FDA UDI | Class II | Active |
| Curaplex | 8600-01120 | FDA UDI | Class II | Active |
| Curaplex | 2-0211-8132 | FDA UDI | Class I | Active |
| Curaplex | 8600-NASCNA-1487 | FDA UDI | Class I | Active |
| Curaplex | 2811-05530 | FDA UDI | Class I | Active |
| Curaplex® | 2442-BVMPAA | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MAC-35 | FDA UDI | Class I | Active |
| Curaplex | 2145-13503 | FDA UDI | Class I | Active |
| Curaplex | 8600-IV016G-1213 | FDA UDI | Class II | Active |
| Curaplex | 8600-01418 | FDA UDI | Class II | Active |
| Curaplex | 2113-20365 | FDA UDI | Class II | Active |
| Curaplex | 020037 | FDA UDI | Class I | Active |
| Curaplex | 670104-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-10265 | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 3271-300LSEP | FDA UDI | Class I | Active |
| Curaplex | 301-PSC125 | FDA UDI | Class I | Active |
| Curaplex | B853 | FDA UDI | Class I | Active |
| Curaplex | 8600-01364 | FDA UDI | Class II | Active |
| Curaplex | 8600-01479 | 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 |