Skip to content

APIFIX LTD

US Last updated 23 May 2026

Is this your brand? Sign in to claim this brand

Devices
43
Registries
GUDIDFDA
FDA recalls
0

Catalogue43

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Apifix Ltd Yokneam Elit, Northern · IL FEI 3013461531

What APIFIX LTD makes

APIFix Ltd manufactures spinal fixation hardware, including non-bioabsorbable bone screws and mechanical distraction rods designed for spinal alignment. Their products also include extenders for these rods, intended for use in minimally invasive deformity correction procedures. The Minimally Invasive Deformity Correction (MID-C) System is a core offering, incorporating these components for surgical applications.

The company’s devices are classified under Class II (N) in the FDA’s regulatory framework and are listed in the FDA’s Unique Device Identification (UDI) database. These products are intended for use in the United States, adhering to applicable FDA requirements for spinal fixation systems. The manufacturer is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does APIFix Ltd manufacture?

APIFix Ltd specializes in spinal fixation hardware, including non-bioabsorbable spinal bone screws, mechanical distraction rods, and mechanical spinal distraction rod extenders. These devices are primarily designed for use in minimally invasive deformity correction procedures, such as the Minimally Invasive Deformity Correction (MID-C) System, which combines these components for surgical applications.

Where is APIFix Ltd based?

APIFix Ltd is headquartered in the United States. The company’s location aligns with its focus on manufacturing and distributing devices intended for use in the US market, where regulatory compliance with the FDA is applicable.

Which regulatory registries list APIFix Ltd’s devices?

APIFix Ltd’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures traceability and transparency for spinal fixation systems, including the company’s products like the MID-C System, which are classified under Class II (N) in the FDA’s regulatory framework.

How are APIFix Ltd’s devices classified by regulatory authorities?

APIFix Ltd’s devices fall under Class II (N) classification in the FDA’s regulatory system. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as spinal fixation hardware used in surgical procedures.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
DUNS number
649220688