DESIGN • ENGINEER • MANUFACTURE • INSTALL • MAINTAIN

Turnkey · FDA Compliant · Made in USA

Custom-Engineered Hyperbaric Systems

PCCI delivers turnkey hyperbaric facilities and systems with end-to-end guidance to help your program perform at its best.

Hyperbaric Systems

Custom-engineered hyperbaric systems tailored to user-design specifications with end-to-end turnkey guidance.

Multiplace Chambers

Medical-rated, rectangular or cylindrical chambers for 2-30 people with single to triple lock configurations. Baseline models available.

Monoplace Chambers

New Althea 4200 Model for upright, seated treatment OR certified, preowned chambers.

Equine Chambers

Large veterinary chambers built for equine or dromedary recovery therapy.

Hypobaric / Altitude chambers

Altitude simulation systems for military and aerospace research applications.

Mobile Trailer Systems

Monoplace or multiplace trailered chamber systems for mobile treatment applications.

Tunneling Chambers

Medical lock chambers for controlled decompression in compressed-air tunneling operations.

SAFETY & CODE COMPLIANCE

Certified Quality. Engineered to Perform.

ASME Pressure Vessel & Boiler Code (PVBC)

All pressure vessels associated with PCCI Hyperbaric Chamber Systems are built to ASME PVBC, Section VIII, Div. 1 for certified structural integrity.

ASME Pressure Vessel Human Occupancy-1 (PVHO-1)

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

NFPA-99 Compliant Fire Suppression Systems

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

ISO 9001-2015 Quality Management System (QMS)

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

FDA 510(k) Compliant

PCCI clinical hyperbaric chambers are FDA 510(k) cleared, certifying design and fabrication processes meet the U.S. FDA 21 CFR Pt. 820 requirements.

Made in the USA

Designed, engineered, and manufactured domestically.

SERVICES

Full Lifecycle Management

HBOT Facility Site Design

Turnkey Chamber Design & Fabrication

Installation and Training

Recertification & Resale

Preventative & Corrective Maintenance

Facility Inspections & Upgrades

Applications

Hyperbaric Oxygen Therapy for Every Mission

45+ Years. One Trusted Hyperbaric Lineage.

PCCI acquired Reimers Systems in 2018, carrying forward its pioneering legacy in hyperbaric engineering with expanded resources and support.

FAQ's

FAQ's

PCCI Hyperbaric Systems designs, engineers, manufactures, installs and maintains hyperbaric and hypobaric chamber systems in the USA. Its product line covers multiplace, monoplace, equine, mobile trailer, tunneling, altitude and research chambers, supported by facility design, staff training, recertification and maintenance services for the full life of each system.
A monoplace chamber treats one patient at a time in a compact single-person vessel. A multiplace chamber holds several patients plus an inside attendant, is pressurized with air while patients breathe oxygen through hoods or masks, and lets staff enter or exit while the chamber stays under pressure. Multiplace systems suit high patient volumes and critical care.
Yes. PCCI designs and fabricates its hyperbaric chambers in the United States and is an FDA-registered medical device manufacturer. Pressure vessels are built to ASME Section VIII Division 1, patient vessels to ASME PVHO-1, and fire suppression systems to NFPA 99 Chapter 14, under an ISO 9001:2015 quality management system.
A clinical hyperbaric chamber in the US is generally expected to meet ASME PVHO-1 for pressure vessels for human occupancy, ASME Section VIII Division 1 for the pressure vessel, NFPA 99 Chapter 14 for the hyperbaric facility, and FDA medical device requirements, plus any state and local building and fire codes.
Yes. PCCI Hyperbaric Systems is an FDA-registered medical device manufacturer, and its medical multiplace chambers are FDA 510(k) cleared. Its Althea 4200 monoplace chamber is listed in the FDA’s Global Unique Device Identification Database (GUDID) as a device in commercial distribution.