Telltale, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Telltale, LLC - FDA 510(k) Cleared Devices
Recent clearances: TELLTALE Electrosurgical Guidewire System
1
Total
1
Cleared
0
Denied
Telltale, LLC has 1 FDA 510(k) cleared medical devices. Based in Andover, US.
Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Telltale, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Telltale, LLC
1 devices