Plexus Yoga, LLC Dba Chirp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plexus Yoga, LLC Dba Chirp - FDA 510(k) Cleared Devices
Recent clearances: TENS&EMS units (SM9109A, SM9109B)
1
Total
1
Cleared
0
Denied
Plexus Yoga, LLC Dba Chirp has 1 FDA 510(k) cleared medical devices. Based in Lehi, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Plexus Yoga, LLC Dba Chirp Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Plexus Yoga, LLC Dba Chirp
1 devices