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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 24 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 670223-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01365 | FDA UDI | Class II | Active |
| Curaplex | 8600-01419 | FDA UDI | Class I | Active |
| Curaplex | 2202 | FDA UDI | Class I | Active |
| Curaplex | 8600-01093 | FDA UDI | Class II | Active |
| Curaplex | 8600-01302 | FDA UDI | Class II | Active |
| Curaplex | 2113-20355 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-030S | FDA UDI | Class I | Active |
| Curaplex | 8600-01389 | FDA UDI | Class I | Active |
| Curaplex | 301-44F50-100 | FDA UDI | Class II | Active |
| Curaplex | 36090 | FDA UDI | Class II | Active |
| Curaplex | 8600-01342 | FDA UDI | Class II | Active |
| Curaplex | 1121-36549 | FDA UDI | Class I | Active |
| Curaplex | 8600-01340 | FDA UDI | Class II | Active |
| Curaplex | BLS-8705KIT | FDA UDI | Class II | Active |
| Curaplex | B1115 | FDA UDI | Class I | Active |
| Curaplex | 8600-01258 | FDA UDI | Class I | Active |
| Curaplex | CUR-PEL100 | FDA UDI | Class I | Active |
| Curaplex | 670006-KIT | FDA UDI | Class I | Active |
| Curaplex | 1212-12105 | FDA UDI | Class I | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2761-32701 | FDA UDI | Class II | Active |
| Curaplex | 2114-19303 | FDA UDI | Class I | Active |
| Curaplex | 8600-4X4PAD-12106 | FDA UDI | Class II | Active |
| Curaplex | 62241518S | FDA UDI | Class II | Active |
| Curaplex | 1715-01837 | FDA UDI | Class II | Active |
| Curaplex | 2114-04085-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-FO-RS-0 | FDA UDI | Class I | Active |
| Curaplex | 1121-36567 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-1015S | FDA UDI | Class I | Active |
| Curaplex | 1612-84110 | FDA UDI | Class II | Active |
| Curaplex | 8600-01462 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-Y | FDA UDI | Class I | Active |
| Curaplex | 8600-01380 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-MAC-35-S | FDA UDI | Class I | Active |
| Curaplex | 1014 | FDA UDI | Class II | Active |
| Curaplex | 2113-10270 | FDA UDI | Class II | Active |
| Curaplex | 15-10411 | FDA UDI | Class II | Active |
| Curaplex | 8600-01274 | FDA UDI | Class II | Active |
| Curaplex | 2113-10200 | FDA UDI | Class II | Active |
| Curaplex | 8600-ADUNRB-1376 | FDA UDI | Class I | Active |
| Curaplex | 021169-2S | FDA UDI | Class I | Active |
| Curaplex | B2000 | FDA UDI | Class I | Active |
| Curaplex | 18575MS | FDA UDI | Class I | Active |
| Curaplex | 670265-KIT | FDA UDI | Class II | Active |
| Curaplex | 30071 | FDA UDI | Class II | Active |
| Curaplex | 8600-012012 | FDA UDI | Class I | Active |
| Curaplex | LA8641-C | FDA UDI | Class I | Active |
| Curaplex | KLTSD403K | FDA UDI | Class I | Active |
| Curaplex | 1015-47146 | 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 |