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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
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020460367
- DUNS Number
- —
Catalogue (2165)
Page 29 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01216 | FDA UDI | Class II | Active |
| Curaplex | B854 | FDA UDI | Class I | Active |
| Curaplex | 1860-08783 | FDA UDI | Class II | Active |
| Curaplex | 2113-20280 | FDA UDI | Class II | Active |
| Curaplex | 301-100EA | FDA UDI | Class I | Active |
| Curaplex | 8600-01298 | FDA UDI | Class II | Active |
| Curaplex | 29310-S | FDA UDI | Class I | Active |
| Curaplex | 660223 | FDA UDI | Class II | Active |
| Curaplex | 670146-KIT | FDA UDI | Class II | Active |
| Curaplex | 540-1358-A | FDA UDI | Class II | Active |
| Curaplex | TA-UOM | FDA UDI | Class II | Active |
| Curaplex | 677538 | FDA UDI | Class II | Active |
| Curaplex | 670220-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01407 | FDA UDI | Class I | Active |
| Curaplex | 1215-22196 | FDA UDI | Class I | Active |
| Curaplex | 8600-01240 | FDA UDI | Class II | Active |
| Curaplex | 8600-01321 | FDA UDI | Class I | Active |
| Curaplex | 2430-26955 | FDA UDI | Class II | Active |
| Curaplex | 670034-KIT | FDA UDI | Class II | Active |
| Curaplex | 2514-007QM | FDA UDI | Class I | Active |
| Curaplex | XT605-BK-EN | FDA UDI | Class I | Active |
| Curaplex | 670084-KIT | FDA UDI | Class II | Active |
| Curaplex | 2010-34080 | FDA UDI | Class I | Active |
| Curaplex | 8600-01279 | FDA UDI | Class II | Active |
| Curaplex | 670122-KIT | FDA UDI | Class I | Active |
| Curaplex | TC3B-A-HL-ST | FDA UDI | Class I | Active |
| Curaplex | 8600-01395 | FDA UDI | Class I | Active |
| Curaplex | 1460-003QM | FDA UDI | Class I | Active |
| Curaplex | 1860-08705 | FDA UDI | Class II | Active |
| Curaplex | 670141-KIT | FDA UDI | Class I | Active |
| Curaplex | 2-0211-4680 | FDA UDI | Class I | Active |
| Curaplex | 2113-10340 | FDA UDI | Class II | Active |
| Curaplex | 660203 | FDA UDI | Class II | Active |
| Curaplex | 2101 | FDA UDI | Class I | Active |
| Curaplex | 1004SPCO | FDA UDI | Class I | Active |
| Curaplex | 5-0236-09 | FDA UDI | Class I | Active |
| Curaplex | 3271-60402EA | FDA UDI | Class I | Active |
| Curaplex | N6997 | FDA UDI | Class I | Active |
| Curaplex | 8600-01194 | FDA UDI | Class I | Active |
| Curaplex | 2114-04082-KIT | FDA UDI | Class II | Active |
| Curaplex® | SGOPAPMD01-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-10270 | FDA UDI | Class II | Active |
| Curaplex | TC3CB-A-HL-CAT | FDA UDI | Class I | Active |
| Curaplex | 670137-KIT | FDA UDI | Class II | Active |
| Curaplex | 670195-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-15-S | FDA UDI | Class I | Active |
| Curaplex | 8600-01484 | FDA UDI | Class I | Active |
| Curaplex | 670022-KIT | FDA UDI | Class I | Active |
| Curaplex | 670176-KIT | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | 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 |