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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 22 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 662131 | FDA UDI | Class II | Active |
| Curaplex | B1010 | FDA UDI | Class I | Active |
| Curaplex | 351631-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01323 | FDA UDI | Class I | Active |
| Curaplex | 1121-36559 | FDA UDI | Class I | Active |
| Curaplex | EMP4000RBC | FDA UDI | Class I | Active |
| Curaplex | 36003 | FDA UDI | Class I | Active |
| Curaplex® | 1015-47150 | FDA UDI | Class I | Active |
| Curaplex | 8600-01415 | FDA UDI | Class II | Active |
| Curaplex | 2021-15132 | FDA UDI | Class I | Active |
| Curaplex | 36013 | FDA UDI | Class II | Active |
| Curaplex | 30071 | FDA UDI | Class II | Active |
| Curaplex | TC1B-B-CP-ST | FDA UDI | Class II | Active |
| Curaplex | 8600-01421 | FDA UDI | Class II | Active |
| Curaplex | 670181-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-20335 | FDA UDI | Class II | Active |
| Curaplex | 2430-26956 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-100M | FDA UDI | Class I | Active |
| Curaplex | 301-LED-PH1-M | FDA UDI | Class I | Active |
| Curaplex | 1460-004QM | FDA UDI | Class I | Active |
| Curaplex | 8600-01296 | FDA UDI | Class II | Active |
| Curaplex | 2114-19301 | FDA UDI | Class I | Active |
| Curaplex | 681229 | FDA UDI | Class II | Active |
| Curaplex | TA-DEP | FDA UDI | Class II | Active |
| Curaplex | 36274 | FDA UDI | Class I | Active |
| Curaplex® | 8600-01534 | FDA UDI | Class I | Active |
| Curaplex | 301-184 | FDA UDI | Class I | Active |
| Curaplex | 670244-KIT | FDA UDI | Class II | Active |
| Curaplex | 1840-20142-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01350 | FDA UDI | Class II | Active |
| Curaplex | 670275-KIT | FDA UDI | Class I | Active |
| Curaplex | 5107F-SE | FDA UDI | Class II | Active |
| Curaplex | 36151 | FDA UDI | Class II | Active |
| Curaplex | 1012-47123 | FDA UDI | Class I | Active |
| Curaplex | 2113-20285 | FDA UDI | Class II | Active |
| Curaplex | 533-MS-25060EA | FDA UDI | Class I | Active |
| Curaplex | 1612-84140 | FDA UDI | Class II | Active |
| Curaplex | MD300CN310 | FDA UDI | Class II | Active |
| Curaplex | 1841-14012 | FDA UDI | Class I | Active |
| Curaplex | 8600-01309 | FDA UDI | Class II | Active |
| Curaplex | 661420 | FDA UDI | Class II | Active |
| Curaplex | 670191-KIT | FDA UDI | Class I | Active |
| Curaplex | 1012-47135R | FDA UDI | Class I | Active |
| Curaplex | 8600-01330 | FDA UDI | Class I | Active |
| Curaplex | 1012-47125R | FDA UDI | Class I | Active |
| Curaplex | 660222 | FDA UDI | Class II | Active |
| Curaplex | 670217-KIT | FDA UDI | Class II | Active |
| Curaplex | G4500BK | FDA UDI | Class I | Active |
| Curaplex | B1020 | FDA UDI | Class I | Active |
| Curaplex | 16714 | 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 |