FDA 510(k) Applications Submitted by Lumenis Be Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K250809 | 03/17/2025 | Stellar M22 | Lumenis Be Ltd. |
| K242349 | 08/08/2024 | FoLix | Lumenis Be Ltd. |
| K233301 | 09/29/2023 | ULTRApulse Alpha CO2 Laser System, Delivery Devices and Accessories | Lumenis Be Ltd. |
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