Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011687221

FEI Number

3011687221

Entity Name

FOOTSCIENTIFIC, INC.

City/State/Country

Draper, UT, US

Establishment Address

76 W 13775 S STE 4, Draper, UT 84020, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

FootScientific, Inc. (Owner Number: 10049593)

Owner / Operator Contact Address

76 W 13775 S, #4, Draper, UT 84020, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Elevate® by FootScientific® Elevate Child® by FootScientific Flex AFO by FlintRehab Hammer Toe Fusion Reamer FuseRight

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHI	Orthosis, Foot Drop	Physical Medicine	Class 1	890.3475	2015-06-24
HTO	Reamer	Orthopedic	Class 1	888.4540	2019-12-09

Official Correspondent

Chris Hughes

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FootScientific, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0021-2015	Biomet, Inc.	1	Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011687221. Last updated year: 2026. Please use registration number 3011687221 when referencing this establishment in official correspondence.