Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008872348

FEI Number

3008872348

Entity Name

STRUTZ, INC

City/State/Country

Englewd Clfs, NJ, US

Establishment Address

650 E Palisade Ave Ste 2-103, Englewd Clfs, NJ 07632, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

STRUTZ, Inc (Owner Number: 10034950)

Owner / Operator Contact Address

650 E.Palisade Ave, Ste 2-103, Englewood Cliffs, NJ 07632, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Strutz Sole Angel

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQI	Orthosis, Limb Brace	Physical Medicine	Class 1	890.3475	2011-01-19

Official Correspondent

Steven Llorens

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STRUTZ, Inc

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008872348. Last updated year: 2026. Please use registration number 3008872348 when referencing this establishment in official correspondence.