FDA Database
71,174 reports · 32 product codes · Updated weekly
28 results for “watchman”
BOSTON SCIENTIFIC CORPORATION, MARINA BAY CUST. FULFILLMENT CENTER
Left Atrial Appendage Closure
UNKNOWN
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
BOSTON SCIENTIFIC CORPORATION
Left Atrial Appendage Closure
Claripulse monitors these devices weekly and detects anomalies using 6 statistical methods — spike, trend, changepoint, peer-outlier, and more.
Get Early AccessNew to MAUDE?
MAUDE (Manufacturer and User Facility Device Experience) is the FDA's public database of medical device adverse event reports submitted by manufacturers, importers, device user facilities, and the public. It is the most comprehensive public source of device safety reports in the United States.
Yes. This lookup tool is free to use. It reads the same publicly available openFDA data and refreshes weekly.
We pull from the openFDA API every week, so the device counts and timelines reflect the most recent reports the FDA has published.
No. MAUDE is passive surveillance, so report counts reflect reporting behavior rather than true event rates. Counts can be affected by sales volume, publicity, and recalls. Use the data to spot patterns worth investigating, not to rank devices by safety.
This tool covers 32 cardiac device types across eight categories, including pacemakers and ICDs, ablation catheters, TAVR and structural heart devices, coronary stents, and mechanical circulatory support devices such as Impella and LVADs.
