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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 42 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1432-56000 | FDA UDI | Class I | Active |
| Curaplex | 8600-01332 | FDA UDI | Class II | Active |
| Curaplex | 5-5333-57 | FDA UDI | Class I | Active |
| Curaplex | 2113-10350 | FDA UDI | Class II | Active |
| Curaplex | 670219-KIT | FDA UDI | Class II | Active |
| Curaplex | 14762MS | FDA UDI | Class II | Active |
| Curaplex | 8600-01149 | FDA UDI | Class II | Active |
| Curaplex | 1122-14962 | FDA UDI | Class I | Active |
| Curaplex | 670210-KIT | FDA UDI | Class II | Active |
| Curaplex | 621011 | FDA UDI | Class II | Active |
| Curaplex | 30054 | FDA UDI | Class I | Active |
| Curaplex | 2010-35090 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MIL-000-M | FDA UDI | Class I | Active |
| Curaplex | 670065-KIT | FDA UDI | Class II | Active |
| Curaplex | FCBLF-RED | FDA UDI | Class I | Active |
| Curaplex | 2113-20335 | FDA UDI | Class II | Active |
| Curaplex | 3141-91012 | FDA UDI | Class I | Active |
| Curaplex | 2115-11504 | FDA UDI | Class I | Active |
| Curaplex | AS-TRK-A-CAT | FDA UDI | Class II | Active |
| Curaplex | 2113-10260 | FDA UDI | Class II | Active |
| Curaplex | 2525-61323 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MAC-4-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01446 | FDA UDI | Class II | Active |
| Curaplex | 2141-13510 | FDA UDI | Class I | Active |
| Curaplex | 69100MS | FDA UDI | Class II | Active |
| Curaplex | 301-PSC114 | FDA UDI | Class I | Active |
| Curaplex | 2114-193025 | FDA UDI | Class I | Active |
| Curaplex® | 8600-01522 | FDA UDI | Class II | Active |
| Curaplex | 8600-01087 | FDA UDI | Class II | Active |
| Curaplex | 36162 | FDA UDI | Class II | Active |
| Curaplex® | 1015-47153 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-8124 | FDA UDI | Class I | Active |
| Curaplex | 68101S | FDA UDI | Class II | Active |
| Curaplex | 301-103 | FDA UDI | Class I | Active |
| Curaplex | 8600-01497 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-0-S | FDA UDI | Class I | Active |
| Curaplex | 670274-KIT | FDA UDI | Class I | Active |
| Curaplex | 1012-47142 | FDA UDI | Class I | Active |
| Curaplex | 30072MS | FDA UDI | Class II | Active |
| Curaplex | 1015-47147 | FDA UDI | Class I | Active |
| Curaplex | 681207 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-3-S | FDA UDI | Class I | Active |
| Curaplex | 3271-63802 | FDA UDI | Class I | Active |
| Curaplex | 8600-01368 | FDA UDI | Class I | Active |
| Curaplex | 1012-47126 | FDA UDI | Class I | Active |
| Curaplex | 301-670253-KIT | FDA UDI | Class I | Active |
| Curaplex | 3246-95206 | FDA UDI | Class I | Active |
| Curaplex | 8600-01445 | FDA UDI | Class I | Active |
| Curaplex | 540-1343EA-A | FDA UDI | Class II | Active |
| Curaplex | 71050 | 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 |