🎉 Share Your 2025 Year-End Summary & Win $10,000 Sharing Rewards!
Reflect on your year with Gate and share your report on Square for a chance to win $10,000!
👇 How to Join:
1️⃣ Click to check your Year-End Summary: https://www.gate.com/competition/your-year-in-review-2025
2️⃣ After viewing, share it on social media or Gate Square using the "Share" button
3️⃣ Invite friends to like, comment, and share. More interactions, higher chances of winning!
🎁 Generous Prizes:
1️⃣ Daily Lucky Winner: 1 winner per day gets $30 GT, a branded hoodie, and a Gate × Red Bull tumbler
2️⃣ Lucky Share Draw: 10
Nyxoah's Genio Scores in Europe: The Sleep Apnea Device Shaking Up Patient Options
Nyxoah SA (NYXH) just kicked off commercial operations in the Netherlands for Genio, its breakthrough implant therapy for obstructive sleep apnea (OSA), with successful initial procedures at OLVG West Amsterdam and Zuyderland Hospital Heerlen. Here’s what makes this matter: OSA affects millions worldwide and carries serious risks—think heart problems, stroke, and even early mortality—but the standard CPAP treatment? Most patients hate wearing it long-term.
Why Genio Stands Out
Genio takes a completely different approach using bilateral hypoglossal nerve stimulation to keep airways open during sleep. The tech is genuinely innovative: it’s leadless, battery-free, runs on external power, and works anywhere an MRI machine exists. That last part matters because competitors can’t do full-body MRI imaging. The system also fires up both sides of the hypoglossal nerve simultaneously, which means it actually works even when you’re flat on your back—a position where many competing devices struggle.
The design philosophy centers on patient experience. Surgeons praise how simple the implant procedure is, and patients get easy upgrades through an external chip. For people dealing with complete concentric collapse (CCC)—a condition that locks them out of competitor options—Genio becomes a genuine alternative.
Regulatory Path & Confidence Builders
The road here involved serious validation. CE Mark came through in 2019, and most recently, FDA approval hit in August 2025 for adult patients with moderate-to-severe OSA. The DREAM IDE study and BETTER SLEEP trial provided the evidence base. Clinical data showed strong tolerability and that the hypoglossal nerve function remained stable and reliable across diverse patient populations.
The Expansion Play
The Netherlands launch is tactical—it’s positioned as a springboard for broader European rollout. Nyxoah is partnering with major medical centers to scale adoption, treating this market entry as a proof-of-concept for commercial scaling.
Stock Action Worth Tracking
NYXH has ranged between $4.34 and $11.87 over the past year. Yesterday closed at $4.80 (down 0.62%), but premarket trading Wednesday showed momentum: up 6% at $5.10. The commercial milestone could fuel investor interest as the company transitions from regulatory phase to revenue generation.