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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 18 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 677556 | FDA UDI | Class II | Active |
| Curaplex | 8600-01311 | FDA UDI | Class II | Active |
| Curaplex | 36187 | FDA UDI | Class II | Active |
| Curaplex | 670201-KIT | FDA UDI | Class I | Active |
| Curaplex® | 670271-KIT | FDA UDI | Class II | Active |
| Curaplex | 301-PSCU114 | FDA UDI | Class I | Active |
| Curaplex | 8600-01499 | FDA UDI | Class I | Active |
| Curaplex | 8600-01181 | FDA UDI | Class II | Active |
| Curaplex | 36010 | FDA UDI | Class II | Active |
| Curaplex | 023080S | FDA UDI | Class II | Active |
| Curaplex | 1431-66000 | FDA UDI | Class I | Active |
| Curaplex | 16106 | FDA UDI | Class II | Active |
| Curaplex | 1841-14011 | FDA UDI | Class I | Active |
| Curaplex | 670171-KIT | FDA UDI | Class II | Active |
| Curaplex | 2-0211-8134 | FDA UDI | Class I | Active |
| Curaplex | MRIPEEP-A | FDA UDI | Class II | Active |
| Curaplex | TC2B-A-ML-CAT | FDA UDI | Class I | Active |
| Curaplex | 8600-01478 | FDA UDI | Class II | Active |
| Curaplex | 10-83011 | FDA UDI | Class II | Active |
| Curaplex | 8600-01287 | FDA UDI | Class I | Active |
| Curaplex | 660205 | FDA UDI | Class II | Active |
| Curaplex | 8600-01227 | FDA UDI | Class I | Active |
| Curaplex | 444002 | FDA UDI | Class II | Active |
| Curaplex | 301-670249-KIT | FDA UDI | Class II | Active |
| Curaplex | 2021-15136 | FDA UDI | Class I | Active |
| Curaplex | 2114-19305 | FDA UDI | Class I | Active |
| Curaplex | 8600-ETTB40-1263 | FDA UDI | Class II | Active |
| Curaplex | 686007-A | FDA UDI | Class I | Active |
| Curaplex | 1012-47136 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-101S | FDA UDI | Class I | Active |
| Curaplex | 680503PHX1 | FDA UDI | Class I | Active |
| Curaplex | 1071-10204 | FDA UDI | Class I | Active |
| Curaplex | 1840-27604-A | FDA UDI | Class II | Active |
| Curaplex | 1122-14964 | FDA UDI | Class I | Active |
| Curaplex | 2113-10290 | FDA UDI | Class II | Active |
| Curaplex | 301-LED-035S | FDA UDI | Class I | Active |
| Curaplex | 8600-01242 | FDA UDI | Class I | Active |
| Curaplex | 670034-KIT-DOD | FDA UDI | Class I | Active |
| Curaplex | SOB1APG-23-KIT | FDA UDI | Class I | Active |
| Curaplex | 15-10411NEG | FDA UDI | Class II | Active |
| Curaplex | 301-0723ANEVALPACK | FDA UDI | Class II | Active |
| Curaplex | 8600-SL1MLS-1436 | FDA UDI | Class II | Active |
| Curaplex | 36277 | FDA UDI | Class I | Active |
| Curaplex | SF-1 | FDA UDI | Class I | Active |
| Curaplex | 2113-20270 | FDA UDI | Class II | Active |
| Curaplex | G4401OK | FDA UDI | Class I | Active |
| Curaplex | 301-180U | FDA UDI | Class I | Active |
| Curaplex | 2811-05529 | FDA UDI | Class I | Active |
| Curaplex | 2113-10280 | FDA UDI | Class II | Active |
| Curaplex | 301-116EA | 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 |