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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 16 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 1340-27000 | FDA UDI | Class I | Active |
| Curaplex | 1212-12103 | FDA UDI | Class I | Active |
| Curaplex | 670033-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-20350 | FDA UDI | Class II | Active |
| Curaplex | 2113-20360 | FDA UDI | Class II | Active |
| Curaplex | 8600-01490 | FDA UDI | Class I | Active |
| Curaplex | 6840155STK | FDA UDI | Class II | Active |
| Curaplex | 670162-KIT-DOD | FDA UDI | Class II | Active |
| Curaplex | 301-BVM550 | FDA UDI | Class II | Active |
| Curaplex | 8600-01136 | FDA UDI | Class II | Active |
| Curaplex | 12307 | FDA UDI | Class II | Active |
| Curaplex | 44200S | FDA UDI | Class II | Active |
| Curaplex | 36100 | FDA UDI | Class II | Active |
| Curaplex | 2113-20290 | FDA UDI | Class II | Active |
| Curaplex | 670167-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01339 | FDA UDI | Class I | Active |
| Curaplex | 670138-KIT | FDA UDI | Class I | Active |
| Curaplex | 1012-44884 | FDA UDI | Class I | Active |
| Curaplex | 8600-01281 | FDA UDI | Class II | Active |
| Curaplex | 8600-01506 | FDA UDI | Class I | Active |
| Curaplex | 16108 | FDA UDI | Class II | Active |
| Curaplex | 8600-01169 | FDA UDI | Class II | Active |
| Curaplex | 2010-36110 | FDA UDI | Class I | Active |
| Curaplex | 8600-ETTB30-1261 | FDA UDI | Class II | Active |
| Curaplex | 8600-EKGLPD-1327 | FDA UDI | Class II | Active |
| Curaplex | 8600-01410 | FDA UDI | Class I | Active |
| Curaplex | 1431-55000 | FDA UDI | Class I | Active |
| Curaplex | 8600-01308 | FDA UDI | Class II | Active |
| Curaplex | 1243-A | FDA UDI | Class II | Active |
| Curaplex | 670238-KIT | FDA UDI | Class II | Active |
| Curaplex | 590500K | FDA UDI | Class II | Active |
| Curaplex | 18315 | FDA UDI | Class II | Active |
| Curaplex | 1712-12345 | FDA UDI | Class II | Active |
| Curaplex | 8600-10CCSY-1439 | FDA UDI | Class II | Active |
| Curaplex | 2113-20295 | FDA UDI | Class II | Active |
| Curaplex | 36096 | FDA UDI | Class II | Active |
| Curaplex | 8600-01349 | FDA UDI | Class II | Active |
| Curaplex | 670236-KIT | FDA UDI | Class II | Active |
| Curaplex | 670027-KIT | FDA UDI | Class I | Active |
| Curaplex | 651777 | FDA UDI | Class II | Active |
| Curaplex | 8600-01295 | FDA UDI | Class I | Active |
| Curaplex | 47525S | FDA UDI | Class I | Active |
| Curaplex | EMSREG8725-B2D-BTM | FDA UDI | Class I | Active |
| Curaplex | 1004SP-A | FDA UDI | Class I | Active |
| Curaplex | 677556-1 | FDA UDI | Class II | Active |
| Curaplex | 3817001P | FDA UDI | Class I | Active |
| Curaplex | TC2CB-A-ML-CAT | FDA UDI | Class I | Active |
| Curaplex | 10-670034-KIT | FDA UDI | Class I | Active |
| Curaplex | 4440010 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-RS-1 | 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 |