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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 1 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 38022 | FDA UDI | Class II | Active |
| Curaplex | AS-TRK-B-CAT | FDA UDI | Class II | Active |
| Curaplex | TC2B-A-ML-ST | FDA UDI | Class I | Active |
| Curaplex | 16250 | FDA UDI | Class II | Active |
| Curaplex | 12992 | FDA UDI | Class II | Active |
| Curaplex | 686505G | FDA UDI | Class II | Active |
| Curaplex | 670215-KIT | FDA UDI | Class II | Active |
| Curaplex | 1072-25001 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-0 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2525-19301 | FDA UDI | Class I | Active |
| Curaplex | 8600-01195 | FDA UDI | Class I | Active |
| Curaplex | 301-8600-01266 | FDA UDI | Class II | Active |
| Curaplex | 661131MS | FDA UDI | Class I | Active |
| Curaplex | 2113-20255 | FDA UDI | Class II | Active |
| Curaplex | 2745-10075 | FDA UDI | Class I | Active |
| Curaplex | 36768 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-25058EA | FDA UDI | Class I | Active |
| Curaplex | 8600-01373 | FDA UDI | Class II | Active |
| Curaplex | 812-CHEST | FDA UDI | Class II | Active |
| Curaplex | 2-0211-4635 | FDA UDI | Class I | Active |
| Curaplex | 670184-KIT | FDA UDI | Class I | Active |
| Curaplex | 2010-34090 | FDA UDI | Class I | Active |
| Curaplex | 1830-12113 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-8130 | FDA UDI | Class I | Active |
| Curaplex | 3271-44100 | FDA UDI | Class I | Active |
| Curaplex | 670007-KIT | FDA UDI | Class I | Active |
| Curaplex | 670234-KIT | FDA UDI | Class I | Active |
| Curaplex | 661565 | FDA UDI | Class II | Active |
| Curaplex | LA8641R | FDA UDI | Class I | Active |
| Curaplex | 301-LED-100S | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 680154-KIT | FDA UDI | Class II | Active |
| Curaplex | 1840-08804-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01391 | FDA UDI | Class I | Active |
| Curaplex | 8600-01090 | FDA UDI | Class I | Active |
| Curaplex | AF4000 | FDA UDI | Class II | Active |
| Curaplex | 670183-KIT | FDA UDI | Class II | Active |
| Curaplex | TTSK-3 | FDA UDI | N | Active |
| Curaplex | B1040 | FDA UDI | Class I | Active |
| Curaplex | 680509 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4650 | FDA UDI | Class I | Active |
| Curaplex | 36276 | FDA UDI | Class I | Active |
| Curaplex® | SGOPAPLG01-24-KIT | FDA UDI | Class II | Active |
| Curaplex | TC1CB-B-CP-CAT | FDA UDI | Class II | Active |
| Curaplex | 1613-86214 | FDA UDI | Class II | Active |
| Curaplex | 8600-01188 | FDA UDI | Class I | Active |
| Curaplex | XT605-BK-EN | FDA UDI | Class I | Active |
| Curaplex | 670147-KIT | FDA UDI | Class II | Active |
| Curaplex | 670194-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 |