Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3036773435

FEI Number

3036773435

Entity Name

GD-STRIDE LTD

City/State/Country

Jerusalem, IL

Establishment Address

216 Jaffo St., Jerusalem 9438307, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GD-Stride LTD (Owner Number: 10092903)

Owner / Operator Contact Address

216 Jaffo St., Jerusalem, IL-JM 9438307, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Phynix

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MNE	Orthosis, Moldable, Supportive, Skin Protective	Physical Medicine	Class 1	890.3475	2025-03-05

Official Correspondent

Daniel Weisz

US Agent Details

Susan Alpert Business: SFA Regulatory C/O Dr Susan Alpert Email: drsusanalpert@gmail.com Phone: (612) 2027019

Related Public Records

Same Entity

GD-Stride LTD

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 3036773435. Last updated year: 2026. Please use registration number 3036773435 when referencing this establishment in official correspondence.