Medical Device Manufacturer · US , Plymouth , MN

Bridge Medical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Recent clearances: CROSSBOSS CATHETER MODEL M-2000, STINGRAY ORIENTING BALLOON CATHETER MODEL M-1000, STINGRAY GUIDEWIRE MODEL M-3004 AND M, BRIDGE SENTRY BEDSIDE UNIT, BRIDGE SENTRY ADMINISTRATION SET-STANDARD CONFIGURATION, BRIDGE SENTRY ADMINISTRATION SET 5

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bridge Medical, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Aug 25, 1998

BRIDGE SENTRY BEDSIDE UNIT, BRIDGE SENTRY ADMINISTRATION SET-STANDARD...

General Hospital · 337d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 08, 2026