Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013461531

FEI Number

3013461531

Entity Name

APIFIX LTD

City/State/Country

Yokneam Elit, Northern, IL

Establishment Address

1 Hacarmel Stree, Kochav Yokneam Bldg, Yokneam Elit, Northern 2069207, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ApiFix LTD (Owner Number: 10062505)

Owner / Operator Contact Address

1 Hacarmel Street Kochav Yokneam Bldg, Yokneam Elit,, IL-Z 2069207, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

H170001

All Registered Proprietary Names

Minimally Invasive Deformity Correction (MID-C) System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QGP	Posterior Ratcheting Rod System	Unknown	Class N	N/A	2020-02-06

Official Correspondent

Adi Prager

US Agent Details

Ray Garrison Email: rgarrison@orthopediatrics.com Phone: (574) 2668637

Related Public Records

Same Entity

ApiFix 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 3013461531. Last updated year: 2026. Please use registration number 3013461531 when referencing this establishment in official correspondence.