Medical Device Manufacturer · US , San Diego , CA

Neuralace Medical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Neuralace Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Jan 2024. Active since 2021. Primary specialty: Physical Medicine.

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

Regulatory submissions have been managed by Acknowledge Regulatory Strategies, LLC and RQM+. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Neuralace Medical, Inc.
2 devices
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All2 Physical Medicine 2