Fillauer Composites

FDA Device Registration & Listing · Salt Lake City, UT, US · Registration 3007510149

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
3007510149
FEI Number
3007510149
Entity Name
Fillauer Composites
City/State/Country
Salt Lake City, UT, US
Establishment Address
3938 S 300 W, Salt Lake City, UT 84107, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FILLAUER COMPANIES, INC. (Owner Number: 9910012)
Owner / Operator Contact Address
2710 AMNICOLA HWY., Chattanooga, TN 37406, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Element K2 Formula SLX Foot Wave El Dorado Climbing Foot AllPro Little Feet Ibex Aeris MX Foot Obsidian

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 2004-04-21

Official Correspondent

Annette Cole

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FILLAUER COMPANIES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1723997 MOTION CONTROL, INC. SALT LAKE CITY, UT, US
9681133 FILLAUER EUROPE JARFALLA Stockholm, SE
1022826 FILLAUER, LLC CHATTANOOGA, TN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007510149. Last updated year: 2026. Please use registration number 3007510149 when referencing this establishment in official correspondence.
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