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TJO launches infection spacer system for revision knee surgery

Nov. 3, 2026
TJO launches infection spacer system for revision knee surgery
By AI, Created 13:00 UTC, Nov 03, 2026, AGP -

Total Joint Orthopedics has launched the Klassic Infection Spacer System, expanding its revision knee line with a device cleared for both temporary and permanent use. The system is set to debut at AAHKS in Texas and is designed to support two-stage infection cases with simpler instrumentation and more stable knee function.

Why it matters: - The launch gives surgeons a new option for periprosthetic joint infection revision cases, where maintaining motion and stability between stages can affect recovery. - KISS is designed to replace molded cement spacers with permanent implant materials, which may improve function and simplify reconstruction in complex knee infections. - The system adds another infection-management tool to TJO’s Klassic Revision Knee platform as the company pushes toward lower instrumentation burden in joint replacement.

What happened: - Total Joint Orthopedics launched the Klassic Infection Spacer System, or KISS, expanding the Klassic Revision Knee System for periprosthetic joint infection revision procedures. - The company said KISS is the first system cleared for a dual indication: permanent implantation and temporary implantation for PJI. - KISS received FDA 510(k) clearance in July 2026 as part of the Klassic Knee System. - The system will debut at the American Association of Hip and Knee Surgeons Annual Meeting, Nov. 5-8, 2026, in Grapevine, Texas. - Surgeons can view the Klassic Infection Spacer, Klassic Revision Knee and Universal Cone Systems at Booth 1503.

The details: - KISS uses permanent implant materials, including Aurum/Ti, CoCr and ultra-high molecular-weight polyethylene. - The system is intended for up to 180 days of temporary use as an adjunct to total knee replacement in patients undergoing a two-stage procedure due to a septic process. - KISS is also indicated for permanent primary or revision total knee arthroplasty procedures. - The system’s modularity includes expanded fixation and augmentation options. - TJO says that design helps deliver a stable, functional knee, preserve range of motion, reduce pain and provide a path to reconstruction. - The Ultra-PS articulating surface uses an ultracongruent design to provide stability through the full range of motion after extensive debridement in many PJI cases. - KISS uses TJO’s Klassic ONE instrumentation and requires a single tray of instruments for up to 90% of cases. - For complete indications, contraindications, warnings and precautions, TJO directs surgeons to the instructions for use at tjoinc.com/ifu.

Between the lines: - The launch extends TJO’s strategy of simplifying joint replacement while keeping a revision-focused product line centered on streamlined instrumentation. - The dual-indication clearance may matter because it lets surgeons use one system across both temporary infection management and later definitive reconstruction. - TJO is also signaling that articulating spacers remain a preferred approach over static options in many knee infection cases, especially when preserving motion is a priority.

What's next: - TJO will use AAHKS as the first public showcase for KISS. - Surgeons are expected to evaluate how the new spacer system fits into two-stage PJI workflows and revision knee reconstruction. - The company will likely position KISS alongside its existing Klassic Knee and Universal Cone offerings as part of a broader revision portfolio.

The bottom line: - KISS gives TJO a purpose-built infection spacer that combines temporary and permanent use in one cleared system, with the goal of making complex knee revision surgery simpler and more functional.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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