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WillowWood Global LLC

US

Last updated September 17, 2026

Information

Country
US
Address
15441 SCIOTO DARBY RD., Mt Sterling, OH, 43143
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1522166
DUNS Number
—

Catalogue (185)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
LimbLogic LLV-02100
FDA UDI
Class IActive
Alpha ACLS-049-M18
FDA UDI
Class IIActive
LimbLogic LLV-2002SU
FDA UDI
Class IActive
Alpha ACL-302
FDA UDI
Class IIActive
Alpha ACL-049-X18
FDA UDI
Class IIActive
Alpha ACL-049-X12
FDA UDI
Class IIActive
Alpha ACL-049-M16
FDA UDI
Class IIActive
LimbLogic LLV-02104
FDA UDI
Class IActive
Alpha ACL-301
FDA UDI
Class IIActive
Alpha ACL-303
FDA UDI
Class IIActive
One ONE-SIDE
FDA UDI
Class IActive
One ONE-TTVD-MP-LG
FDA UDI
Class IActive
Alpha ACL-049-X20
FDA UDI
Class IIActive
One ONE-TF-SIDE-2
FDA UDI
Class IActive
Intuy WW-1LK-1W
FDA UDI
Class IActive
One ONE-TF-SIDE-1
FDA UDI
Class IActive
Alpha ACL-049-M14
FDA UDI
Class IIActive
LimbLogic LLV-2000-S
FDA UDI
Class IActive
Alpha ACLS-049-X06
FDA UDI
Class IIActive
LimbLogic LLV-KIT-P
FDA UDI
Class IActive
LimbLogic LLV-EV2
FDA UDI
Class IActive
Alpha ACLS-049-S10
FDA UDI
Class IIActive
Alpha ACLS-049-X18
FDA UDI
Class IIActive
LimbLogic LLV-21083
FDA UDI
Class IActive
Alpha ACL-049-S22
FDA UDI
Class IIActive
LimbLogic LLV-01071
FDA UDI
Class IActive
One ONE-TTVD-LG-MD
FDA UDI
Class IActive
Alpha ACLS-049-M04
FDA UDI
Class IIActive
LimbLogic LLV21043R
FDA UDI
Class IActive
Alpha ACLS-049-M14
FDA UDI
Class IIActive
Alpha ACLS-049-M22
FDA UDI
Class IIActive
Alpha ACLS-049-X22
FDA UDI
Class IIActive
LimbLogic LLV-01070
FDA UDI
Class IActive
LimbLogic LL-01220
FDA UDI
Class IActive
One ONE-TFVD-LG-S
FDA UDI
Class IActive
Alpha ACL-049-M12
FDA UDI
Class IIActive
Alpha ACLS-049-S22
FDA UDI
Class IIActive
Alpha ACL-049-M06
FDA UDI
Class IIActive
Alpha ACLS-049-S14
FDA UDI
Class IIActive
One ONE-TFVS-XL-D
FDA UDI
Class IActive
LimbLogic LLV-02103
FDA UDI
Class IActive
LimbLogic LLV-02006
FDA UDI
Class IActive
LimbLogic LLV-21043R
FDA UDI
Class IActive
Alpha ACLS-049-S08
FDA UDI
Class IIActive
LimbLogic LLV-21084
FDA UDI
Class IActive
LimbLogic LLV-02101
FDA UDI
Class IActive
LimbLogic LLV-02003
FDA UDI
Class IActive
One ONE-TF-SIDE-3
FDA UDI
Class IActive
Alpha ACL-300
FDA UDI
Class IIActive
LimbLogic LLV-2000-L
FDA UDI
Class IActive

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Authorities

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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.

DateRecall No.ClassStatusReason
Apr 20, 2021Z-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.