Medical Device Manufacturer · US , Mesa , AZ

Ulthera, Inc. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 2009
13
Total
12
Cleared
1
Denied

Ulthera, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Mesa, US.

Latest FDA clearance: May 2025. Active since 2009.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ulthera, Inc.
13 devices
1-13 of 13
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