# Bridge Medical, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 2 (1998–2011): 2 510(k) clearances
- Product codes: DQY (1), FRN (1)
- Predicates its devices cite: 17 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bridgepoint Medical: 6 (https://510kreport.com/company/bridgepoint-medical)
- Lumend, Inc.: 5 (https://510kreport.com/company/lumend)
- Pryor Products: 1 (https://510kreport.com/company/pryor-products)
- Medical Specialties, Inc.: 1 (https://510kreport.com/company/medical-specialties)
- River Medical, Inc.: 1 (https://510kreport.com/company/river-medical)
- Kendall Mcgaw Laboratories, Inc.: 1 (https://510kreport.com/company/kendall-mcgaw-laboratories)
- Baxa Corp., Sub. of Cook Group, Inc.: 1 (https://510kreport.com/company/baxa-sub-of-cook-group)
- Y: 1 (https://510kreport.com/company/y)

## Firms that cite its devices most
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Bridgepoint Medical: 2 (https://510kreport.com/company/bridgepoint-medical)
- Nitiloop, Ltd.: 1 (https://510kreport.com/company/nitiloop)

## Its most-cited devices
- K102725: Crossboss Catheter Model M-2000, Stingray Orienting Balloon Catheter Model M-1000, Stingray Guidewire Model M-3004 and M (2011), cited by 5

## Recent decisions
- K102725: Crossboss Catheter Model M-2000, Stingray Orienting Balloon Catheter Model M-1000, Stingray Guidewire Model M-3004 and M (May 10, 2011)
- K973593: Bridge Sentry Bedside Unit, Bridge Sentry Administration Set-Standard Configuration, Bridge Sentry Administration Set 5 (Aug 25, 1998)

Source page: https://510kreport.com/company/bridge-medical