Atraverse Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atraverse Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HOTWIRE RF GUIDEWIRE (901XXX), HOTWIRE™ System RF Generator and Footswitch (optional accessory)
2
Total
2
Cleared
0
Denied
Atraverse Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Cardiff By The Sea, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Atraverse Medical, Inc. 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 - Atraverse Medical, Inc.
2 devices