Pensar Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pensar Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: PocketDoc™ Micro Wound Therapy System
2
Total
2
Cleared
0
Denied
Pensar Medical, LLC has 2 FDA 510(k) cleared medical devices. Based in Temecula, US.
Historical record: 2 cleared submissions from 2016 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pensar Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pensar Medical, LLC
2 devices