Medical Device Manufacturer · US , Beverly Hills , CA

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

8 submissions · 8 cleared · Since 2022
8
Total
8
Cleared
0
Denied

Pearl, Inc. has 8 FDA 510(k) cleared medical devices. Based in Beverly Hills, US.

Latest FDA clearance: Nov 2025. Active since 2022. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Pearl, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Boston Medtech Advisors as regulatory consultant.

FDA 510(k) Regulatory Record - Pearl, Inc.
8 devices
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