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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 41 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 14781 | FDA UDI | Class I | Active |
| Curaplex | 563500 | FDA UDI | Class I | Active |
| Curaplex | 8600-01235 | FDA UDI | Class II | Active |
| Curaplex | 44250S | FDA UDI | Class I | Active |
| Curaplex | 533-MS-25058EA | FDA UDI | Class I | Active |
| Curaplex | 301-0923A | FDA UDI | Class II | Active |
| Curaplex | 8600-SSC10F-1378 | FDA UDI | Class I | Active |
| Curaplex | 8600-01486 | FDA UDI | Class II | Active |
| Curaplex | 1841-009QM | FDA UDI | Class I | Active |
| Curaplex | 670050-KIT | FDA UDI | Class II | Active |
| Curaplex | 670279-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-4-S | FDA UDI | Class I | Active |
| Curaplex | 670096-KIT | FDA UDI | Class II | Active |
| Curaplex | 2525-31618 | FDA UDI | Class II | Active |
| Curaplex | 660787-US | FDA UDI | Class I | Active |
| Curaplex | 30051 | FDA UDI | Class I | Active |
| Curaplex | AEG100 | FDA UDI | Class I | Active |
| Curaplex | 1612-84220 | FDA UDI | Class II | Active |
| Curaplex | 507650 | FDA UDI | Class I | Active |
| Curaplex | 2909005XL | FDA UDI | Class II | Active |
| Curaplex | 777556 | FDA UDI | Class II | Active |
| Curaplex | 8600-01137 | FDA UDI | Class I | Active |
| Curaplex | BT-42604 | FDA UDI | Class I | Active |
| Curaplex | 14068EA | FDA UDI | Class I | Active |
| Curaplex | 8600-03CCSY-1440 | FDA UDI | Class II | Active |
| Curaplex | 2114-16301 | FDA UDI | Class I | Active |
| Curaplex | 2113-20355 | FDA UDI | Class II | Active |
| Curaplex | 660788-MB-CAT | FDA UDI | Class I | Active |
| Curaplex | 670125-KIT | FDA UDI | Class I | Active |
| Curaplex | 301-0207 | FDA UDI | Class I | Active |
| Curaplex | 021169-1S | FDA UDI | Class I | Active |
| Curaplex | 301-150 | FDA UDI | Class I | Active |
| Curaplex | 8600-01288 | FDA UDI | Class II | Active |
| Curaplex | 8600-01467 | FDA UDI | Class I | Active |
| Curaplex | 1841-14008 | FDA UDI | Class I | Active |
| Curaplex | 36092 | FDA UDI | Class II | Active |
| Curaplex | 1121-36572 | FDA UDI | Class I | Active |
| Curaplex® | 1015-47154 | FDA UDI | Class I | Active |
| Curaplex | 2113-20200 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-000S | FDA UDI | Class I | Active |
| Curaplex | 1612-84240 | FDA UDI | Class II | Active |
| Curaplex | 8600-ETTB65-1268 | FDA UDI | Class II | Active |
| Curaplex | 295814 | FDA UDI | Class I | Active |
| Curaplex | 8600-01493 | FDA UDI | Class I | Active |
| Curaplex | 670241-KIT | FDA UDI | Class II | Active |
| Curaplex | 670233-KIT | FDA UDI | Class I | Active |
| Curaplex | 680123-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01438 | FDA UDI | Class I | Active |
| Curaplex | B3200 | FDA UDI | Class I | Active |
| Curaplex | 8600-01376 | 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 |