Fabrication Enterprises Inc 00-2026 Knee Cpm Unit

Product Description

The FABRICATION ENTERPRISES INC 00-2026 is a continuous passive motion (CPM) device designed for postoperative knee rehabilitation. Weighing 23 pounds and measuring only 37 inches in length, it is a lightweight and compact unit suited for clinical and home-based recovery protocols. The device delivers passive knee joint movement across a range of motion from -10 to 120 degrees, helping to reduce stiffness, limit scar tissue formation, and maintain joint mobility following knee surgery. An on-board power supply and single screw drive mechanism contribute to straightforward operation. A licensed physical therapist, occupational therapist, or durable medical equipment specialist typically oversees setup and patient instruction.

The 00-2026 is intended for postoperative knee patients in both outpatient clinical and home settings. It accommodates patients from 4 feet to 6.6 feet in height. The reversible footplate allows adjustment for shorter leg lengths, broadening the range of patients the unit can serve. A wide, low-profile closed-base frame provides stability during use. The standard hand control enables the patient to adjust speed and range within clinician-defined limits, while the patient lockout feature prevents modification of prescribed settings without authorization.

Key Features

• Lightweight at 23 pounds for easy transport and setup in clinical or home environments
• Compact 37-inch length for use in standard hospital beds and home settings
• Range of motion from -10 to 120 degrees for comprehensive postoperative protocols
• Reversible footplate accommodates shorter leg lengths
• Patient lockout feature maintains clinician-prescribed ROM and speed settings
• On-board power supply eliminates the need for a separate external transformer
• Interchangeable hand controls for versatility across patient needs

Compatibility

Designed for use with adult patients ranging from 4 feet to 6.6 feet in height. Compatible with interchangeable hand controls for the OptiFlex-K1 platform.

Installation Notes

Setup and patient fitting should be performed by a qualified clinician or trained DME technician following the manufacturer instructions. Power down the unit before adjusting limb supports or changing hand controls. Ensure the base frame is placed on a stable, flat surface before initiating motion cycles. Patient ROM and speed parameters should be configured by a licensed provider before enabling patient-operated controls.