Lumenis Limited
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| FemTouch delivery system includes the FemTouch Kit (AC-1007415) and FemTouch" Tip (SPSA-20 recall (Z-0301-2017) | Lumenis Limited | 2016-10-23 |
| Light Sheer Desire Diode Laser System with XC Handpiece Accessory options. recall (Z-1519-2015) | Lumenis Limited | 2015-04-24 |
| The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or recall (Z-0795-2013) | Lumenis Limited | 2013-02-14 |
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Every clearance here is in the API, with alerts when new ones post.