Bridge Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Bridge Medical, Inc. makes
Bridge Medical, Inc. manufactures interventional cardiology devices, including the CROSSBOSS Catheter (Model M-2000) for coronary atherectomy, the STINGRAY Orienting Balloon Catheter (Model M-1000) for vessel preparation, and STINGRAY Guided Wires (Models M-3004 and M) for coronary navigation. The company also produces the BRIDGE SENTRY Bedside Unit and associated administration sets (Standard and 5-unit configurations) for managing thrombolytic therapy in acute myocardial infarction.
These devices are classified as Class II under the US FDA regulatory framework and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Bridge Medical, Inc. have in the registry?
The registry currently lists 2 devices for Bridge Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bridge Medical, Inc.'s devices?
Among its 2 most recently registered devices, Bridge Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bridge Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bridge Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bridge Medical, Inc. in the registry?
The most recently registered devices listed for Bridge Medical, Inc. include CROSSBOSS CATHETER MODEL M-2000, STINGRAY ORIENTING BALLOON CATHETER MODEL M-1000, STINGRAY GUIDEWIRE MODEL M-3004 AND M and BRIDGE SENTRY BEDSIDE UNIT, BRIDGE SENTRY ADMINISTRATION SET-STANDARD CONFIGURATION, BRIDGE SENTRY ADMINISTRATION SET 5.