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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 20 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2145-13405 | FDA UDI | Class I | Active |
| Curaplex | 1860-08702 | FDA UDI | Class II | Active |
| Curaplex | B4023 | FDA UDI | Class I | Active |
| Curaplex | 670204-KIT | FDA UDI | Class I | Active |
| Curaplex | 670182-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01186 | FDA UDI | Class I | Active |
| Curaplex | B4020 | FDA UDI | Class I | Active |
| Curaplex | B-3030 | FDA UDI | Class I | Active |
| Curaplex | 301-107EA | FDA UDI | Class I | Active |
| Curaplex | 2145-13400 | FDA UDI | Class I | Active |
| Curaplex | 670061-KIT | FDA UDI | Class II | Active |
| Curaplex | 2-0211-4675 | FDA UDI | Class I | Active |
| Curaplex | 2442-20100 | FDA UDI | Class II | Active |
| Curaplex | 301-44F10-120 | FDA UDI | Class II | Active |
| Curaplex | 8600-01322 | FDA UDI | Class I | Active |
| Curaplex | 1012-44986 | FDA UDI | Class I | Active |
| Curaplex | 8600-01095 | FDA UDI | Class I | Active |
| Curaplex | 1121-36573 | FDA UDI | Class I | Active |
| Curaplex | 64250 | FDA UDI | Class II | Active |
| Curaplex | 3246-95204 | FDA UDI | Class I | Active |
| Curaplex | 670246-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01494 | FDA UDI | Class I | Active |
| Curaplex | 8600-01207 | FDA UDI | Class II | Active |
| Curaplex | 1012-47124 | FDA UDI | Class I | Active |
| Curaplex | 670086-KIT | FDA UDI | Class II | Active |
| Curaplex | 2113-10345 | FDA UDI | Class II | Active |
| Curaplex | 677555-1 | FDA UDI | Class II | Active |
| Curaplex | 2430-19010 | FDA UDI | Class II | Active |
| Curaplex | 8600-FLSHES-1220 | FDA UDI | Class II | Unknown |
| Curaplex | 351215 | FDA UDI | Class II | Active |
| Curaplex | 301-PrO2LT-FM | FDA UDI | Class II | Active |
| Curaplex | 301-1014 | FDA UDI | Class I | Active |
| Curaplex | TC-MMCB1CG1A0GBBT | FDA UDI | Class I | Active |
| Curaplex | 8600-01475 | FDA UDI | Class II | Active |
| Curaplex | 2525-15411 | FDA UDI | Class III | Active |
| Curaplex | 8600-01255 | FDA UDI | Class II | Active |
| Curaplex | NC200 | FDA UDI | Class I | Active |
| Curaplex | 8600-01277 | FDA UDI | Class II | Active |
| Curaplex | 2021-15020 | FDA UDI | Class I | Active |
| Curaplex | 8600-01271 | FDA UDI | Class I | Active |
| Curaplex | 2115-01980 | FDA UDI | Class II | Active |
| Curaplex | 8600-01125 | FDA UDI | Class II | Active |
| Curaplex | 8600-01047 | FDA UDI | Class II | Active |
| Curaplex | B1030 | FDA UDI | Class I | Active |
| Curaplex | B5110 | FDA UDI | Class I | Active |
| Curaplex | 2113-20360 | FDA UDI | Class II | Active |
| Curaplex | 1840-011QM | FDA UDI | Class II | Active |
| Curaplex | 2114-16304 | FDA UDI | Class I | Active |
| Curaplex | 301-PrO2LTEZ-MF | FDA UDI | Class II | Active |
| Curaplex | 533-MS-MED5N | FDA UDI | Class II | 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 |