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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 12 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | BT-42612 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-0-M | FDA UDI | Class I | Active |
| Curaplex | 1122-14960 | FDA UDI | Class I | Active |
| Curaplex | MRIPEEP | FDA UDI | Class II | Active |
| Curaplex | 3271-62002 | FDA UDI | Class I | Active |
| Curaplex | 36002 | FDA UDI | Class I | Active |
| Curaplex | 1124-32400 | FDA UDI | Class I | Active |
| Curaplex | TA3000 | FDA UDI | Class I | Active |
| Curaplex | 2113-10350 | FDA UDI | Class II | Active |
| Curaplex | CUR5603 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LT-MSA | FDA UDI | Class II | Active |
| Curaplex | TC2B-B-ML-CAT | FDA UDI | Class I | Active |
| Curaplex | 1777-S | FDA UDI | Class II | Active |
| Curaplex | 301-8600-01267 | FDA UDI | Class II | Active |
| Curaplex | 2525-NSCCBAG | FDA UDI | Class II | Active |
| Curaplex | 301-FO-PH1-S | FDA UDI | Class I | Active |
| Curaplex | 1121-36563 | FDA UDI | Class I | Active |
| Curaplex | 2741-50484 | FDA UDI | Class II | Active |
| Curaplex | 36279 | FDA UDI | Class I | Active |
| Curaplex | 617-8500PKG | FDA UDI | Class II | Active |
| Curaplex | 1121-36556 | FDA UDI | Class I | Active |
| Curaplex | 3271-03490EP | FDA UDI | Class I | Active |
| Curaplex | 670225-KIT | FDA UDI | Class II | Active |
| Curaplex | 2-0211-8128 | FDA UDI | Class I | Active |
| Curaplex | 301-130EA | FDA UDI | Class I | Active |
| Curaplex | 8600-01100 | FDA UDI | Class II | Active |
| Curaplex | 36168 | FDA UDI | Class II | Active |
| Curaplex | 670179-KIT | FDA UDI | Class I | Active |
| Curaplex | 023090S | FDA UDI | Class II | Active |
| Curaplex | 1124-03680 | FDA UDI | Class I | Active |
| Curaplex | 2145-13502 | FDA UDI | Class I | Active |
| Curaplex | 677557-1 | FDA UDI | Class II | Active |
| Curaplex | 8600-01455 | FDA UDI | Class I | Active |
| Curaplex | 1841-14007 | FDA UDI | Class I | Active |
| Curaplex | 05-00100NEG | FDA UDI | Class II | Active |
| Curaplex | 8600-EMESIS-1545 | FDA UDI | Class I | Active |
| Curaplex | 8600-01167 | FDA UDI | Class I | Active |
| Curaplex | 1612-84145 | FDA UDI | Class II | Active |
| Curaplex | 670224-KIT | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4690 | FDA UDI | Class I | Active |
| Curaplex | 670222-KIT | FDA UDI | Class I | Active |
| Curaplex | 670041-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01280 | FDA UDI | Class II | Active |
| Curaplex | B1100 | FDA UDI | Class I | Active |
| Curaplex | 8600-01118 | FDA UDI | Class II | Active |
| Curaplex | TC3B-I-HL-CAT | FDA UDI | Class I | Active |
| Curaplex | 8600-01234 | FDA UDI | Class II | Active |
| Curaplex | 8600-01435 | FDA UDI | Class II | Active |
| Curaplex | 301-PSC10715 | FDA UDI | Class I | Active |
| Curaplex | BTM4SHELF | 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 |