Baylis Medical Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
3
Cleared
0
Denied
Baylis Medical Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Latest FDA clearance: Jan 2026. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Baylis Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Baylis Medical Technologies, Inc.
5 devices
Cleared
Jan 18, 2026
Baylis Connector Cable
Cardiovascular
30d
Cleared
Oct 28, 2025
PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch
General & Plastic Surgery
270d
Cleared
Sep 11, 2025
PowerWire® 14 Radiofrequency Guidewire Kit
Cardiovascular
149d
Cleared
Feb 28, 2024
PowerWire Radiofrequency Guidewire Kit
Cardiovascular
188d
Cleared
May 30, 2023
RFP-100A Connector Cable (Single Use)
Cardiovascular
90d