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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 32 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 12995 | FDA UDI | Class II | Active |
| Curaplex® | 1015-47163 | FDA UDI | Class I | Active |
| Curaplex | 8600-SSC14F-1378 | FDA UDI | Class I | Active |
| Curaplex | NSS2003N | FDA UDI | Class II | Active |
| Curaplex | 12992 | FDA UDI | Class II | Active |
| Curaplex | 2212-11200 | FDA UDI | Class II | Active |
| Curaplex | 670230-KIT | FDA UDI | Class I | Active |
| Curaplex | 1612-84250 | FDA UDI | Class II | Active |
| Curaplex | NSSBISHCC | FDA UDI | Class II | Active |
| Curaplex | 30079 | FDA UDI | Class II | Active |
| Curaplex | 2113-10250 | FDA UDI | Class II | Active |
| Curaplex | 660487 | FDA UDI | Class II | Active |
| Curaplex | 1071-10208 | FDA UDI | Class I | Active |
| Curaplex | 670208-KIT | FDA UDI | Class II | Active |
| Curaplex | 670090-KIT | FDA UDI | Class I | Active |
| Curaplex | 3271-63202 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LTEZ-MM | FDA UDI | Class II | Active |
| Curaplex | 2113-20295 | FDA UDI | Class II | Active |
| Curaplex | 30557 | FDA UDI | Class II | Active |
| Curaplex® | 301-5107BVM | FDA UDI | Class II | Active |
| Curaplex | 301-180EA | FDA UDI | Class I | Active |
| Curaplex | 1840-41127 | FDA UDI | Class II | Active |
| Curaplex | 2021-15128 | FDA UDI | Class I | Active |
| Curaplex | 3271-36805 | FDA UDI | Class I | Active |
| Curaplex | 1212-12107 | FDA UDI | Class I | Active |
| Curaplex | 662157 | FDA UDI | Class I | Active |
| Curaplex | SIVSTTAFT-23-KIT | FDA UDI | Class II | Active |
| Curaplex | OneScope Pro | FDA UDI | Class I | Active |
| Curaplex | 2114-04081-KIT | FDA UDI | Class II | Active |
| Curaplex | 14761 | FDA UDI | Class II | Active |
| Curaplex | TC-DLBL23CG1A1GCBH | FDA UDI | Class I | Active |
| Curaplex® | SRXEPI-24-KIT | FDA UDI | N | Active |
| Curaplex | 1712-00359 | FDA UDI | Class II | Active |
| Curaplex | 2113-20345 | FDA UDI | Class II | Active |
| Curaplex | B-3040 | FDA UDI | Class I | Active |
| Curaplex | 2113-10245 | FDA UDI | Class II | Active |
| Curaplex | 660424-500 | FDA UDI | Class II | Active |
| Curaplex | 8600-01315 | FDA UDI | Class II | Active |
| Curaplex | 1712-00360 | FDA UDI | Class II | Active |
| Curaplex | 2113-20290 | FDA UDI | Class II | Active |
| Curaplex | 812-BVMNEBKIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01366 | FDA UDI | Class I | Active |
| Curaplex | 1612-84140 | FDA UDI | Class II | Active |
| Curaplex | 1121-36554 | FDA UDI | Class I | Active |
| Curaplex | 62241515S | FDA UDI | Class II | Active |
| Curaplex | 8600-ETTB55-1266 | FDA UDI | Class II | Active |
| Curaplex | 8600-01460 | FDA UDI | Class I | Active |
| Curaplex | SEEIFAKKIT | FDA UDI | Class I | Active |
| Curaplex® | SGOPAPMD02-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 670203-KIT | FDA UDI | Class I | Active |
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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 |