WillowWood Global LLC

FDA Device Registration & Listing · Mt Sterling, OH, US · Registration 1522166

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1522166
FEI Number
1522166
Entity Name
WillowWood Global LLC
City/State/Country
Mt Sterling, OH, US
Establishment Address
15441 SCIOTO DARBY RD., Mt Sterling, OH 43143, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
WillowWood Global LLC (Owner Number: 1522166)
Owner / Operator Contact Address
15441 SCIOTO DARBY RD., P.O. BOX 130, Mount Sterling, OH 43143, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Alpha Control Liner Valve, multiple LimbLogic VS Alignment component, multiple Limb Cover, multiple Alpha Liner Alpha Basic Liner Alpha SmartTemp Liner Alpha Design Liner WillowWood Express Liner Alpha Hybrid Liner Alpha Silicone Liner Alpha Duo Liner Alpha Classic Liner TruSeal Liner

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2023-03-17
ISP Valve, Prosthesis Physical Medicine Class 1 890.3420 2009-08-28
IQO Device, Prosthesis Alignment Physical Medicine Class 1 890.3025 2009-08-28
IPM Cover, Limb Physical Medicine Class 1 890.3025 2008-10-16

Official Correspondent

Steve Huggins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WillowWood Global LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3035765256 WW-West Mesa, AZ, US
3038873185 Xtremity by WillowWood Global Golden, CO, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K070612 Top-Rank Health Care Equipment Co., Ltd. TOP-RANK ADHESIVE ELECTRODE 2007-05-07
K123915 Grass Technologies, an Astro-Med, Inc. Product Gro DE48-PLUS 2013-04-24
K073532 Technomed Europe DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES 2008-05-01
K260363 Ceribell, Inc. Ceribell Brain Monitor Headband 2026-04-03
K091762 Covidien DURA-STICK SELF-ADHESIVE ELECTRODES WITH ALOE 2009-12-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1522166. Last updated year: 2026. Please use registration number 1522166 when referencing this establishment in official correspondence.
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