WW-West

FDA Device Registration & Listing · Mesa, AZ, US · Registration 3035765256

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
3035765256
FEI Number
3035765256
Entity Name
WW-West
City/State/Country
Mesa, AZ, US
Establishment Address
8743 E Pecos Rd, Mesa, AZ 85212, 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

Prosthetic Foot/Ankle, multiple Impulse SACH Single Axis Meta Shock Meta Arc Meta Shock X Meta Core KOA LP META Flow

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISH Component, External, Limb, Ankle/Foot Physical Medicine Class 1 890.3420 1992-06-23

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
3038873185 Xtremity by WillowWood Global Golden, CO, US
1522166 WillowWood Global LLC Mt Sterling, OH, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035765256. Last updated year: 2026. Please use registration number 3035765256 when referencing this establishment in official correspondence.
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