• Skip to main content
  • Skip to secondary menu
  • Skip to primary sidebar
  • Skip to footer
  • MANUFACTURERS
  • HEADHUNTERS
  • COMPANIES

SPINEMarketGroup

Spine Industry News

  • HOME
  • 2026
  • 2025
  • 2024
  • BROCHURES
  • ARTICLES
  • PRODUCT LIBRARY

ZygoFix Receives FDA Clearance for its zLOCK Lumbar Facet Fixation System

May 6, 2024 By SPINEMarketGroup

Misgav, Israel, 06 May 2024 – ZygoFix Ltd. a portfolio company of The Trendlines Group Ltd. (“Trendlines”) announced  that it received regulatory clearance from the United States Food and Drug Administration (FDA clearance) for its zLOCK Lumbar Facet Fixation System. This achievement was supported by compelling clinical evidence from the company’s ongoing European clinical study, marking a significant advancement in spinal fusion technology.

Spinal fusion, a common surgical procedure performed for degenerative spinal conditions such as Spondylolisthesis, Spinal Stenosis, and degenerative disc disease, traditionally requires placement of 4 screws and 2 rods, creating an artificial bridge, to stabilize the segment. The conventional invasive approach requires precise placement and building of bridges intraoperatively.  ZygoFix’s revolutionary zLOCK system harnesses the spine’s innate bone structure to securely lock its connecting joints.  Unlike traditional methods, the company’s innovative implant adapts to the joint’s anatomy during insertion, offering unparalleled stability with a minimally invasive, simple procedure that can be performed in outpatient and ASC environments.

With CE certification and six years of clinical utilization yielding long-term pain reduction and bone growth, ZygoFix’s zLOCK Lumbar Facet Fixation System is positioned to revolutionize spinal fusion surgery. 

ZygoFix CEO Ofer Levy remarked, “Receiving FDA clearance for our zLOCK Lumbar Stabilization System is an exciting milestone, and I am very proud of the team that has worked hard to achieve this goal.  The system has garnered significant interest in the US market and this clearance paves the way for us to introduce our transformative solution to the US market, fostering collaboration with leading surgeons and enhancing patient care.”

Dr. Nicholas Pachuda, ZygoFix Chair added: “Obtaining 510(k) clearance is a testament to ZygoFix’s commitment to innovation and addressing the unmet needs of patients suffering from degenerative spinal conditions. We eagerly anticipate offering patients our minimally invasive, life-changing solution in the United States.”

Dr. Isador Lieberman,  Orthopedic & Spine Surgeon at Texas Back Institute commented: “The simplicity and minimally invasive nature of the zLOCK system provides a new tool in the surgeon’s offering. For the right patients, zLOCK can provide a great alternative to pedicle screws.”

About ZygoFix 
ZygoFix Ltd. is a spine device company, a portfolio company of the Trendlines Group (SGX: 42T; OTCQX: TRNLY) and has been supported by the Israel Innovation Authority and the European EIC program, alongside The Trendlnes Group and investors worldwide.  The Company’s inventions enable internal joint stabilization while conforming to the joint’s anatomy.

Contact Information 

Ofer Levy, CEO ZygoFix

ofer@zygofix.com

Related Posts:

  • FFX® Becomes the First Facet Cage Cleared by the FDA…
  • FFX® Receives FDA Clearance for Cervical Facet…
  • SC MEDICA Announces Landmark FDA Clearance For Its…

Filed Under: NEWS Tagged With: 2024

Primary Sidebar

PLATINUM SPONSORS

EXALTA 2LOGO-min
GLOBAL biomedica
NORMED newLOGO-min
GENESYS SPINE
SPINEGUARD2025
Dymicron 2
GSMEDICAL2025
spinewaygroup
RUTHLESS SPINE
RUDISHAUER
NGMEDICAL
LfC
ispine
CENTINEL SPINE
TSUNAMI MEDICAL
syntropiq logo
A-SPINE
L&Kmodelo log

POPULAR POST LAST 90 DAYS

  • Globus Medical: Stronger in Spine, but Could DePuy…
  • BROCHURES
  • DePuy Synthes for Sale: Who Could Actually Buy the…
  • Is DePuy Back in the Spine Fight? Why DePuy Really…
  • Highridge Medical CEO Departure: Spine’s…
  • Boston Scientific Puts $1.5 Billion on MiRus: Why…
  • Globus Medical: Strong Q1, Weak Stock Reaction — Is…
  • (2025 Update): Market, Leading FDA-Approved Devices,…
  • (UPDATED 2025): 6 Artificial Cervical Discs You’ll…
  • Modular Pedicle Screws: When Adaptability Becomes…
  • Strong Surgery, Soft Quarter: ATEC and the Cost of…
  • COMPANIES
  • Autonomous Pedicle Screw Placement: Is Spine…
  • (UPDATED 2026) More Than 100 Options, No Single…
  • The Giant Next Door: Is Mindray Spine’s Next…
  • Cervical Fusion Implant Denials: Why Spine Societies…
  • DePuy Synthes Acquires Expanding Innovations™
  • Hospital Access Is Gone. What Comes Next for Spine…
  • Top 60+ Minimally Invasive Sacroiliac Joint Fusion…
  • VB Spine Announces VB Spine Solutions, a…
  • What Is Medtronic’s PILAR™ Technique?
  • Sublaminar Bands in Spine Surgery: Why This Small…
  • Johnson & Johnson Explores Potential $20B Sale…
  • Percutaneous MIS Spine Systems: Why Adoption Still…
  • PRODUCT LIBRARY
  • Globus Medical Reports First Quarter 2026 Results
  • Who Is PAULA, and Why Should Every Deformity Surgeon…
  • L&K Spine Performs First U.S. Deformity Case…
  • Orthopedics Is Moving Into Pain. Zimmer and Globus…
  • VB Spine Signs Master Agreement with Apolo Medica
  • LAST 5 VIDEOS PUBLISHED

    1. Mighty Oak: Acorn 3D™
    2. Syntropiq: Lyra
    3. ATEC Spine: SafeOp®
    4. REACH Medical: Expandable PLIF/TLIF Cage
    5. Expanding Innovations: X-PAC®TLIF 

    Footer

    Contact us:

    spinemarketgroup@gmail.com info@thespinemarketgroup.com

    • LinkedIn
    • Twitter
    • YouTube

    PRIVACY POLICY

    • Legal
    • PRODUCT LIBRARY

    Copyright © 2026 · SPINEMarketGroup