Is this your brand? Sign in to claim ownership.
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 10 of 44| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curaplex | 8600-01504 | FDA UDI | Class I | Active |
| Curaplex | 1840-25310-A | FDA UDI | Class II | Active |
| Curaplex | B5100 | FDA UDI | Class I | Active |
| Curaplex | F1652BAG-A | FDA UDI | Class I | Active |
| Curaplex | 8600-IV022G-1216 | FDA UDI | Class II | Active |
| Curaplex | 36612 | FDA UDI | Class II | Active |
| Curaplex | FCB-CLF | FDA UDI | Class I | Active |
| Curaplex | 590411 | FDA UDI | Class I | Active |
| Curaplex | 8600-SSC08F-1378 | FDA UDI | Class I | Active |
| Curaplex | 301-181EA | FDA UDI | Class I | Active |
| Curaplex | 1121-36570 | FDA UDI | Class I | Active |
| Curaplex | 8600-SSC18F-1378 | FDA UDI | Class I | Active |
| Curaplex | 8600-01209 | FDA UDI | Class II | Active |
| Curaplex | 301-FO-MIL-00-M | FDA UDI | Class I | Active |
| Curaplex | SRxOD2SY-24-KIT | FDA UDI | N | Active |
| Curaplex | 661318 | FDA UDI | Class I | Active |
| Curaplex | 95001 | FDA UDI | Class I | Active |
| Curaplex | 18268 | FDA UDI | Class II | Active |
| Curaplex | 8600-01432 | FDA UDI | Class II | Active |
| Curaplex | B-3010 | FDA UDI | Class I | Active |
| Curaplex | 661133 | FDA UDI | Class I | Active |
| Curaplex | 301-113EA | FDA UDI | Class I | Active |
| Curaplex | 301-12218 | FDA UDI | Class I | Active |
| Curaplex | 1840-38001-A | FDA UDI | Class I | Active |
| Curaplex | 684244C | FDA UDI | Class II | Active |
| Curaplex | 73320 | FDA UDI | Class II | Active |
| Curaplex | 670202-KIT | FDA UDI | Class I | Active |
| Curaplex | 661524 | FDA UDI | Class I | Active |
| Curaplex | 13302 | FDA UDI | Class II | Active |
| Curaplex | B40200 | FDA UDI | Class I | Active |
| Curaplex | 2113-10335 | FDA UDI | Class II | Active |
| Curaplex | 8600-01357 | FDA UDI | Class II | Active |
| Curaplex | 8600-01259 | FDA UDI | Class I | Active |
| Curaplex | 8600-01428 | FDA UDI | Class I | Active |
| Curaplex | 8600-01166 | FDA UDI | Class I | Active |
| Curaplex | 8600-01130 | FDA UDI | Class I | Active |
| Curaplex | 533-MS-25058EA | FDA UDI | Class I | Active |
| Curaplex | 670012-KIT | FDA UDI | Class I | Active |
| Curaplex | 1212-12109 | FDA UDI | Class I | Active |
| Curaplex | 2114-163015 | FDA UDI | Class I | Active |
| Curaplex | 2811-05531 | FDA UDI | Class I | Active |
| Curaplex | 2115-60202 | FDA UDI | Class II | Active |
| Curaplex | 2751-50487 | FDA UDI | Class II | Active |
| Curaplex | 14757MS | FDA UDI | Class II | Active |
| Curaplex | 2114-040815-KIT | FDA UDI | Class II | Active |
| Curaplex | B800 | FDA UDI | Class I | Active |
| Curaplex | 2010-34100 | FDA UDI | Class I | Active |
| Curaplex | 8600-01299 | FDA UDI | Class I | Active |
| Curaplex | F879600-A | FDA UDI | Class II | Active |
| Curaplex | 8600-01338 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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 |