About Us | Zdeer

 

About Zdeer

Founded in 2014, Zdeer is a health-tech brand dedicated to home & family health.
We run on a dual-engine model — "Tech-Medical + Healthy Living":
Tech-Medical — solving "big problems for a few": hearing aids, home health monitors, hair-growth devices,  and other medical-grade products.
Healthy Living — solving "small problems for many": facial care device, oral spray, and other high-frequency wellness products.

 

Our Mission

Guided by the philosophy of "slow, gentle living" and the principle "right people, right products, right deeds," Zdeer rebuilds the medical-device category through a consumer-electronics mindset.
We believe professional-grade health care should be simple, affordable, and dignified — so that better hearing, better sleep, and better living are within everyone's reach.

 

Milestones & Recognition

• FDA Clearance: Bone-conduction hearing aid received FDA 510(k) clearance in June 2026 (K260452, Class II). Zdeer holds both NMPA (China) and FDA clearance for this product category. FDA clearance does not constitute FDA endorsement
• Patents: 3,600+ patent applications filed (China), including 200+ invention-patent applications in the hearing-aid category
• Medical Registrations: Nearly 40 Class II medical device registration certificates (NMPA, China)
• Market Leadership: #1 in online hearing-aid sales in China (Frost & Sullivan, 2025 report); #1 nationwide in China for three consecutive years (Shangpu Consulting, 2026); over 50% share of China's online hearing-aid market (per the cited reports)
• Awards: Red Dot Design Award for two consecutive years (2025 and 2026); two iF Design Awards (for specific Zdeer products)
• Global Reach: Users in 160+ countries (as of 2026), supported by a dedicated international team

 

Join the Zdeer Community

Better health starts at home. Follow us and stay connected for product updates, hearing-health tips, and a journey toward slower, gentler, and healthier living for the whole family.

 

Disclaimer

FDA 510(k) clearance means the device has been determined to be substantially equivalent to a legally marketed predicate device; it does not constitute FDA endorsement.