Xtremity by WillowWood Global

FDA Device Registration & Listing · Golden, CO, US · Registration 3038873185

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
3038873185
FEI Number
3038873185
Entity Name
Xtremity by WillowWood Global
City/State/Country
Golden, CO, US
Establishment Address
15794 West Sixth Street, Frontage Road, Golden, CO 80401, 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

Xtremity Custom Sockets

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISS Prosthesis, Thigh Socket, External Component 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
3035765256 WW-West Mesa, AZ, 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 3038873185. Last updated year: 2026. Please use registration number 3038873185 when referencing this establishment in official correspondence.
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