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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 13 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 2741-50486 | FDA UDI | Class II | Active |
| Curaplex | 3271-62402 | FDA UDI | Class I | Active |
| Curaplex® | 1015-47161 | FDA UDI | Class I | Active |
| Curaplex | 1013 | FDA UDI | Class II | Active |
| Curaplex | TC-SMCB1CG1D1GBCH | FDA UDI | Class I | Active |
| Curaplex | 1071-10206 | FDA UDI | Class I | Active |
| Curaplex | 301-0923B | FDA UDI | Class II | Active |
| Curaplex | 8600-01250 | FDA UDI | Class II | Active |
| Curaplex | 8600-01392 | FDA UDI | Class I | Active |
| Curaplex | 670168-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01481 | FDA UDI | Class I | Active |
| Curaplex | 301-FO-PH-2 | FDA UDI | Class I | Active |
| Curaplex | 8600-01502 | FDA UDI | Class I | Active |
| Curaplex | 71051 | FDA UDI | Class II | Active |
| Curaplex® | 8600-01518 | FDA UDI | Class II | Active |
| Curaplex | 670144-KIT-DOD | FDA UDI | Class II | Active |
| Curaplex | 2525-30318BL | FDA UDI | Class I | Active |
| Curaplex | 670232-KIT | FDA UDI | Class I | Active |
| Curaplex | 1612-84245 | FDA UDI | Class II | Active |
| Curaplex | 16251 | FDA UDI | Class II | Active |
| Curaplex | 8600-01291 | FDA UDI | Class II | Active |
| Curaplex | B5040 | FDA UDI | Class I | Active |
| Curaplex | 2909004XL | FDA UDI | Class II | Active |
| Curaplex | 36184 | FDA UDI | Class II | Active |
| Curaplex | 1612-84145 | FDA UDI | Class II | Active |
| Curaplex | 8600-01485 | FDA UDI | Class I | Active |
| Curaplex | 2113-10275 | FDA UDI | Class II | Active |
| Curaplex | 1121-36555 | FDA UDI | Class I | Active |
| Curaplex | 3141-91010 | FDA UDI | Class I | Active |
| Curaplex | 8600-01182 | FDA UDI | Class II | Active |
| Curaplex | 670142-KIT | FDA UDI | Class I | Active |
| Curaplex | 1612-84140 | FDA UDI | Class II | Active |
| Curaplex | 2145-13505 | FDA UDI | Class I | Active |
| Curaplex | 1012-47127 | FDA UDI | Class I | Active |
| Curaplex | 8600-AFD-AS-KIT | FDA UDI | Class I | Active |
| Curaplex | 38020 | FDA UDI | Class II | Active |
| Curaplex | 36278 | FDA UDI | Class I | Active |
| Curaplex | 2-0211-8120 | FDA UDI | Class I | Active |
| Curaplex | 2514-006QM | FDA UDI | Class I | Active |
| Curaplex | 683924 | FDA UDI | Class I | Active |
| Curaplex | 2114-16303 | FDA UDI | Class I | Active |
| Curaplex | 2114-12002 | FDA UDI | Class II | Active |
| Curaplex | SEEFRKIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01323 | FDA UDI | Class I | Active |
| Curaplex | B4011 | FDA UDI | Class I | Active |
| Curaplex | 8600-01228 | FDA UDI | Class I | Active |
| Curaplex® | 670270-KIT | FDA UDI | Class II | Active |
| Curaplex | CUR5601 | FDA UDI | Class I | Active |
| Curaplex | 36029 | FDA UDI | Class I | Active |
| Curaplex | 36147-HEARTSAFE | 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 |