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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 34 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | B1210 | FDA UDI | Class I | Active |
| Curaplex | 8600-01159 | FDA UDI | Class II | Active |
| Curaplex | 16105 | FDA UDI | Class II | Active |
| Curaplex | 301-143EA | FDA UDI | Class I | Active |
| Curaplex | 1613-862202 | FDA UDI | Class II | Active |
| Curaplex | 301-110EA | FDA UDI | Class I | Active |
| Curaplex | 38015 | FDA UDI | Class II | Active |
| Curaplex | 382000GC | FDA UDI | Class I | Active |
| Curaplex | 8600-01226 | FDA UDI | Class I | Active |
| Curaplex | 2160-20500 | FDA UDI | Class II | Active |
| Curaplex | 670024-KIT | FDA UDI | Class II | Active |
| Curaplex | 2114-040825-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01089 | FDA UDI | Class I | Active |
| Curaplex | 3271-44125 | FDA UDI | Class I | Active |
| Curaplex | 30556 | FDA UDI | Class II | Active |
| Curaplex | 2741-50485 | FDA UDI | Class II | Active |
| Curaplex | 2113-20365 | FDA UDI | Class II | Active |
| Curaplex | 16383 | FDA UDI | Class II | Active |
| Curaplex | 2525-13121 | FDA UDI | Class II | Active |
| Curaplex | 8600-IV014G-1212 | FDA UDI | Class II | Active |
| Curaplex | 670080-KIT | FDA UDI | Class II | Active |
| Curaplex | G4401BK | FDA UDI | Class I | Active |
| Curaplex | 8600-01441 | FDA UDI | Class I | Active |
| Curaplex® | SCPAPMD303-24-KIT | FDA UDI | Class II | Active |
| Curaplex | 662115 | FDA UDI | Class I | Active |
| Curaplex | 8600-01492 | FDA UDI | Class II | Active |
| Curaplex | 8600-01476 | FDA UDI | Class I | Active |
| Curaplex | 301-7100 | FDA UDI | Class II | Active |
| Curaplex | 36111 | FDA UDI | Class I | Active |
| Curaplex | 38017 | FDA UDI | Class II | Active |
| Curaplex | 2113-20365 | FDA UDI | Class II | Active |
| Curaplex | 1052-91611 | FDA UDI | Class II | Active |
| Curaplex | 670261-KIT | FDA UDI | Class I | Active |
| Curaplex | 8600-01290 | FDA UDI | Class II | Active |
| Curaplex | 670268-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-01355 | FDA UDI | Class II | Active |
| Curaplex | 08-08011 | FDA UDI | Class II | Active |
| Curaplex | B2010 | FDA UDI | Class I | Active |
| Curaplex | 1712-00362 | FDA UDI | Class II | Active |
| Curaplex | 1431-77000 | FDA UDI | Class I | Active |
| Curaplex | 301-LED-101M | FDA UDI | Class I | Active |
| Curaplex® | 8600-01520 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-2 | FDA UDI | Class I | Active |
| Curaplex | 670205-KIT | FDA UDI | Class I | Active |
| Curaplex | 2113-10270 | FDA UDI | Class II | Active |
| Curaplex | 670095-KIT | FDA UDI | Class II | Active |
| Curaplex | 8600-ETTB75-1270 | FDA UDI | Class II | Active |
| Curaplex | J8023E | FDA UDI | Class II | Active |
| Curaplex | 670259-KIT | FDA UDI | Class I | Active |
| Curaplex | 1431-16004 | 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 |