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# Oticon Sentio Hearing Device Cleared
- URL: https://www.fdaweb.com/oticon-sentio-hearing-device-cleared/
- Published: 2024-07-12T12:00:00.000Z
- Updated: 2026-09-14T14:35:17.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157341

FDA has cleared an Oticon Medical 510(k) for its active transcutaneous bone conduction hearing system, the Sentio System. The device includes the Sentio 1 Mini, an external sound processor, and Sentio Ti Implant, which is placed under the skin. Its design and slim profile make it 26% lighter than similar marketed devices, according to the company, adding that it provides access to a 360-degree sound experience and offers the widest bandwidth of 9.5kHz.

“Sentio Ti is designed and verified for a higher maximum force output, so that patients can rely on its ability to handle more powerful sound processors,” Oticon says. “From a surgeon’s perspective, the implant is designed for surgical flexibility, ensuring a straightforward procedure.”