Clean Room Packaging

With patient safety dependent in part on the integrity of our packaging, Placon ensures strict adherence to the ISO 13485 certification in Elkhart, IN, at our medical device packaging headquarters, while our Madison and Plymouth facilities each follow ISO 9001 quality control systems. All medical device packaging is also compliant with 21 CFR 820 standards.

Packaging experience that matters

From low to high volume runs, whether developing packaging for orthopaedic implants or cardiac stents, Placon creates innovative medical device packaging systems in our GMP-oriented, lean manufacturing ISO 8 clean room facilities, ensuring package quality and cleanliness. Our experienced engineering, quality and account managers work hand-in-hand with your engineering team to meet tight production specifications and timelines.



Controlled environments

With growing regulatory requirements, sterile pharmaceutical and medical device packaging is produced and packaged in our meticulously controlled ISO certified Class 8 clean room facilities. Our experienced and knowledgeable operations and QA team ensure strict quality control procedures are upheld throughout the entire packaging process from prototyping, thermoforming, welding, die-cutting, printing and packaging. Our protective BargerGard® and pre-validated BargerVPAK™ products are also formed and welded in our clean room environments ensuring production within a controlled environment minimizing contamination.

At Placon we help create medical packaging success stories. With innovative engineering, creative manufacturing and a collaborative environment, it’s a winning combination that puts your needs at the center.

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