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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 3 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1432-67000 | FDA UDI | Class I | Active |
| Curaplex | 38018 | FDA UDI | Class II | Active |
| Curaplex | 1340-40000 | FDA UDI | Class I | Active |
| Curaplex | 536-dynd74260ea-a | FDA UDI | Class II | Active |
| Curaplex | 2812-01927 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MAC-2 | FDA UDI | Class I | Active |
| Curaplex | 670158-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01480 | FDA UDI | Class I | Active |
| Curaplex | CUR5604 | FDA UDI | Class I | Active |
| Curaplex® | FGIVBLOOD02-25-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-20270 | FDA UDI | Class II | Active |
| Curaplex® | 1015-47151 | FDA UDI | Class I | Active |
| Curaplex | 8600-01477 | FDA UDI | Class I | Active |
| Curaplex | 8600-01147 | FDA UDI | Class II | Active |
| Curaplex | 1612-84130 | FDA UDI | Class II | Active |
| Curaplex | 1471-23601 | FDA UDI | Class I | Active |
| Curaplex | 36185 | FDA UDI | Class II | Active |
| Curaplex | AS-TRK-A-ST | FDA UDI | Class II | Active |
| Curaplex | 661138 | FDA UDI | Class I | Active |
| Curaplex | 670248-KIT | FDA UDI | Class II | Active |
| Curaplex | 680121-KIT | FDA UDI | Class II | Active |
| Curaplex | 670052-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01399 | FDA UDI | Class II | Active |
| Curaplex | EMP4SHELF | FDA UDI | Class I | Active |
| Curaplex | 30059 | FDA UDI | Class II | Active |
| Curaplex | 1012-47134 | FDA UDI | Class I | Active |
| Curaplex | 30556 | FDA UDI | Class II | Active |
| Curaplex | 8600-01377 | FDA UDI | Class I | Active |
| Curaplex | 2021-15112 | FDA UDI | Class I | Active |
| Curaplex | 1431-16002 | FDA UDI | Class I | Active |
| Curaplex | 15329 | FDA UDI | Class I | Active |
| Curaplex | 680504 | FDA UDI | Class I | Active |
| Curaplex | 262090P | FDA UDI | Class I | Active |
| Curaplex | 301-183 | FDA UDI | Class I | Active |
| Curaplex | 670207-KIT | FDA UDI | Class I | Active |
| Curaplex | J2234-A | FDA UDI | Class I | Active |
| Curaplex | 12-082461 | FDA UDI | Class I | Active |
| Curaplex® | 2442-BVMPAD-ET | FDA UDI | Class II | Active |
| Curaplex | 670057-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01466 | FDA UDI | Class II | Active |
| Curaplex | 670036-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01463 | FDA UDI | Class II | Active |
| Curaplex® | SSTBCATBC02-24-KIT | FDA UDI | Class I | Active |
| Curaplex | N7281NICKIT | FDA UDI | Class II | Active |
| Curaplex | 670169-KIT | FDA UDI | Class II | Active |
| Curaplex | TC2CB-B-ML-ST | FDA UDI | Class I | Active |
| Curaplex | 1860-08706 | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 1841-14002 | FDA UDI | Class I | Active |
| Curaplex | 683921OD | 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 |