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Sign in to claim this brandWillowWood Global LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 15441 SCIOTO DARBY RD., Mt Sterling, OH, 43143
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1522166
- DUNS Number
- —
Catalogue (185)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LimbLogic | LLVS-2000-S | FDA UDI | Class I | Active |
| LimbLogic | LLV-2000-R | FDA UDI | Class I | Active |
| Alpha | ACLS-049-M10 | FDA UDI | Class II | Active |
| Alpha | ACL-049-M20 | FDA UDI | Class II | Active |
| Alpha | ACL-049-S14 | FDA UDI | Class II | Active |
| One | ONE-TFVD-XL-S | FDA UDI | Class I | Active |
| LimbLogic | LLV-21200 | FDA UDI | Class I | Active |
| One | ONE-TF-DISTAL-DUO-2 | FDA UDI | Class I | Active |
| Alpha | ACL-049-S18 | FDA UDI | Class II | Active |
| One | ONE-TTVD-LP-LG | FDA UDI | Class I | Active |
| LimbLogic | LLV-21044 | FDA UDI | Class I | Active |
| LimbLogic | LLVS-2000-T | FDA UDI | Class I | Active |
| LimbLogic | LLV-2002-T | FDA UDI | Class I | Active |
| LimbLogic | LLV-21011 | FDA UDI | Class I | Active |
| One | ONE-TFVS-XL-S | FDA UDI | Class I | Active |
| LimbLogic | LLV-21085 | FDA UDI | Class I | Active |
| LimbLogic | LLVS-2000-P | FDA UDI | Class I | Active |
| LimbLogic | LLV-2002-L | FDA UDI | Class I | Active |
| One | ONE-TF-SIDE-DUO-4 | FDA UDI | Class I | Active |
| Alpha | ACLS-049-X20 | FDA UDI | Class II | Active |
| Alpha | ACLS-049-S18 | FDA UDI | Class II | Active |
| Alpha | ACL-304 | FDA UDI | Class II | Active |
| Alpha | ACLS-049-M20 | FDA UDI | Class II | Active |
| LimbLogic | LLV-02005 | FDA UDI | Class I | Active |
| LimbLogic | LLVS-2000-L | FDA UDI | Class I | Active |
| LimbLogic | LLV-01050 | FDA UDI | Class I | Active |
| One | ONE-TTVD-MD-MD | FDA UDI | Class I | Active |
| Alpha | ACLS-049-X12 | FDA UDI | Class II | Active |
| LimbLogic | LLVS-ONE-D | FDA UDI | Class I | Active |
| Alpha | ACLS-049-M06 | FDA UDI | Class II | Active |
| Alpha | ACL-049-M04 | FDA UDI | Class II | Active |
| Alpha | ACL-049-XF | FDA UDI | Class II | Active |
| Alpha | ACL-049-X22 | FDA UDI | Class II | Active |
| One | ONE-TFVD-MP-D | FDA UDI | Class I | Active |
| Alpha | ACL-049-S04 | 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 |
|---|---|---|---|---|
| Apr 20, 2021 | Z-1594-2021 | — | open, classified | the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was used in place of the 5/8 pin. Over time, the shorter pin may not engage in either the upper or lower body, causing the cord to come loose or slip which could result in the loss of suspension. |