Jul. 18th, 2024

REACH24H Secures FDA No Objection Letter for rHDPE Recycling Process

News Brief

Hangzhou July 18, 2024 – REACH24H has successfully assisted a leading enterprise in China’s cosmetic and novel material packaging industry in obtaining a No Objection Letter (NOL) from the U.S. Food and Drug Administration (FDA) for the recycling process to produce recycled high-density polyethylene (rHDPE) material.

Why Is Obtaining No Objection Letter (NOL) Important?

The application focused on the physical recycling process of rHDPE (recycled high-density polyethylene), enabling the production of rHDPE suitable for manufacturing 100% recycled-content products. The approved usage conditions fall under E-G (intended for contact with dry foods at room temperature to freezing conditions).


This achievement signifies a major breakthrough for the company in accessing the U.S. recycled plastics market, enhancing brand competitiveness, and marking a critical step toward global market expansion.

Leveraging deep expertise in FDA regulations for recycled plastics and application procedures, REACH24H developed a comprehensive compliance strategy at the project’s outset. Through close collaboration with the client, the team efficiently prepared required documentation and compiled submission dossiers, ultimately securing the NOL approval within a short timeframe.


REACH24H’s Recycled Plastics Compliance Team

REACH24H’s Food Contact Materials (FCM) team offers U.S. recycled plastics registration services, including:

  • Pre-application compliance analysis

  • Dossier preparation and submission

  • Communication with FDA authorities

  • Pre-notification Consultation (PNC) for manufacturers using FDA-certified recycling equipment


Recycled Plastics Compliance Services

United States

  • Compliance analysis report for pre-application assessment

  • Preparation and submission of standard applications (including surrogate contaminant testing)

  • Preparation and submission of Specific Use and Closed-Loop Recycling applications

  • Surrogate contaminant testing supervision

  • FDA communication and PNC inquiries

  • Regulatory updates

European Union

  • Compliance analysis report for EU recycled plastics applications

  • Preparation and submission of EFSA Scientific Opinion (SOL) applications

  • Communication with EFSA authorities

  • Challenge testing supervision

  • Regulatory updates

Full Image