Neuralace Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuralace Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Axon Therapy, Axon Therapy
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