DESIGN • ENGINEER • MANUFACTURE • INSTALL • MAINTAIN
Our turn-key hyperbaric chamber solution begins with a comprehensive design process rooted in your program goals and operational vision. PCCI engineers translate user design specifications into a fully customized chamber and facility plan — purpose-built, code-compliant, and ready for clinical use.
Site design accounts for structural, electrical, plumbing and ventilation requirements, with thoughtful facility outfitting that ensures the space is functional and compliant with all applicable safety codes and regulatory standards.
Four coordinated phases ensure your chamber is engineered, certified, and installed without surprises.

Hyperbaric engineers work with you to capture detailed user design specifications (UDS) — treatment capacity, patient population, workflow — translating those into a fully customized chamber and facility plan.

Chamber fabrication and assembly are executed with precision using premium materials and rigorous quality control to meet FDA, ASME, NFPA, and other governing body requirements.

Once fabrication is complete, the chamber undergoes thorough testing of structural integrity, pressure performance, and all safety and operational systems — fully documented and included with the chamber.

We carefully plan delivery and rigging — navigating access points, weight loads and placement logistics — so the chamber is positioned and anchored with exacting precision.
Every PCCI chamber is fabricated using premium materials and rigorous quality control processes, with full QA/QC documentation delivered alongside the system. From the first 3D model to commissioning, every detail is engineered for safety, longevity, and regulatory peace of mind.

Registered manufacturer per U.S. FDA QMS/ cGMP per 21 CFR, Part 820

The pressure vessel accommodating patients and attendants is built to PVHO-1 standards, the most rigorous for safe human occupancy.

All PCCI multiplace chambers include fire suppression systems compliant with NFPA 99, Chap. 14, Hyperbaric Facilities.

All chambers are designed and fabricated to internationally recognized QMS standard ISO 9001-2015, certifying proven, repeatable processes with consistent results.

Reviewed and backed by licensed Professional Engineers for code compliance, safety, and structural integrity.

Designed, engineered, and manufactured domestically.
Medical-rated, rectangular or cylindrical chambers for 2-30 people with single to triple lock configurations. Baseline models available.
New Althea 4200 Model for upright, seated treatment OR certified, preowned chambers.