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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 30 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 660644 | FDA UDI | Class I | Active |
| Curaplex | 36816 | FDA UDI | Class I | Active |
| Curaplex | MS-001HS | FDA UDI | Class I | Active |
| Curaplex | 8600-01512 | FDA UDI | Class I | Active |
| Curaplex | 71050 | FDA UDI | Class II | Active |
| Curaplex | 14130 | FDA UDI | Class I | Active |
| Curaplex | 1121-36562 | FDA UDI | Class I | Active |
| Curaplex | 1432-56000 | FDA UDI | Class I | Active |
| Curaplex | 670175-KIT | FDA UDI | Class II | Active |
| Curaplex | 2745-10081 | FDA UDI | Class I | Active |
| Curaplex | 2021-15024 | FDA UDI | Class I | Active |
| Curaplex | 1121-36566 | FDA UDI | Class I | Active |
| Curaplex | 590411CB | FDA UDI | Class I | Active |
| Curaplex | 8600-01310 | FDA UDI | Class II | Active |
| Curaplex | 1121-36560 | FDA UDI | Class I | Active |
| Curaplex | 8600-01135 | FDA UDI | Class I | Active |
| Curaplex | 12358 | FDA UDI | Class II | Active |
| Curaplex | 8600-01284 | FDA UDI | Class II | Active |
| Curaplex | 301-670252-KIT | FDA UDI | Class II | Active |
| Curaplex | 670015-KIT | FDA UDI | Class II | Active |
| Curaplex | 681231 | FDA UDI | Class II | Active |
| Curaplex | 8600-01426 | FDA UDI | Class II | Active |
| Curaplex | SEESAK-ECPI | FDA UDI | Class I | Active |
| Curaplex | 36159 | FDA UDI | Class II | Active |
| Curaplex | 2113-10255 | FDA UDI | Class II | Active |
| Curaplex | 8600-G0021 | FDA UDI | Class II | Active |
| Curaplex | 670160-kit | FDA UDI | Class I | Active |
| Curaplex | 8600-01261 | FDA UDI | Class II | Active |
| Curaplex | 1215-22195 | FDA UDI | Class I | Active |
| Curaplex | 10-83011NEG | FDA UDI | Class II | Active |
| Curaplex | 8600-01503 | FDA UDI | Class II | Active |
| Curaplex | 670005-KIT | FDA UDI | Class II | Active |
| Curaplex | 440413 | FDA UDI | Class I | Active |
| Curaplex | 2114-16301 | FDA UDI | Class I | Active |
| Curaplex | 38006 | FDA UDI | Class II | Active |
| Curaplex | 382000OC | FDA UDI | Class I | Active |
| Curaplex | 8600-01371 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-MED3O | FDA UDI | Class II | Active |
| Curaplex | 16380 | FDA UDI | Class II | Active |
| Curaplex | 2113-20280 | FDA UDI | Class II | Active |
| Curaplex | 2113-10290 | FDA UDI | Class II | Active |
| Curaplex | 2113-20260 | FDA UDI | Class II | Active |
| Curaplex | 1841-14001 | FDA UDI | Class I | Active |
| Curaplex | 680151-KIT | FDA UDI | Class II | Active |
| Curaplex | 14756MS | FDA UDI | Class II | Active |
| Curaplex | 670008-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-ETTB25-1260 | FDA UDI | Class II | Active |
| Curaplex | 8600-01180 | FDA UDI | Class I | Active |
| Curaplex | 1004SPCOF | FDA UDI | Class II | Active |
| Curaplex | 8600-01206 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
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Notified Bodies
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Authorities
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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 |