Surgalign has 45 days to avoid being delisted from Nasdaq, the company said April 14.

The first cases with Curiteva's 3D-printed Inspire Porous PEEK HAFuse cervical interbody system were completed, the devicemaker said April 14.

Stryker spine's former Vice President and General Manager Lane Major was named president and CEO of Grenova, a life sciences company.

Centinel Spine's global motion preservation sales reached $13 million in the fourth quarter of 2022, the devicemaker said April 12. 

Implanet's SqualeTM anterior cervical cage received FDA 510(k) approval, the devicemaker said April 11. 

The second clinical case using ZSFab's cervical interbody system was completed by Jeffrey Moore, MD, the devicemaker said April 10.

Community Medical Center in Toms River, N.J. added NuVasive's Pulse spine platform, according to a news release shared in The Link News.

Fernando Villamil, MD, completed the first clinical case with ZSFab's cervical interbody implant, the devicemaker said April 5.

Stryker CEO Kevin Lobo's total compensation grew to about $18.6 million in 2022, according to a recent Securities and Exchange Commission proxy filing.

Spinal Resources recieved FDA approval for its Solutions Based Spine Platform, the devicemaker said April 4.

Aurora Spine received Institutional Review Board approval for a multicenter study of its Dexa-C cervical interbody system.

CereVasc, a medical device company, appointed Adel Malek, MD, PhD, as chief medical officer. 

CoreLink's Siber Ti sacroiliac joint fusion system received FDA 510(k) clearance, the devicemaker said March 29.

Sword Health unveiled an artificial intelligence platform designed to reduce unecessary spine and orthopedic surgeries.

Here are four updates in cervical spine devices and implants since Feb. 1:

Here are three updates on spine medtech mergers and acquisitions since Feb. 28:

Medacta's MySpine software was found to be effective and safe in pedicle screw placement, according to a study in Surgical Technology International.

Surgalign launched its next generation of the Holo Portal spine guidance system, the medtech company said March 20.

Woven Orthopedic Technologies earned FDA 510(k) clearance for its Ogmed implant enhancement system, the devicemaker said March 16.

ZimVie's vertebral body tethering system for scoliosis recieved a positive medical policy decision from Highmark, the devicemaker said March 15.