# Rubicor Medical, Inc.

- Location (FDA's records): San Carlos, CA
- FDA decisions: 8 (2002–2007): 8 510(k) clearances
- Product codes: GEI (6), KNW (2)
- Predicates its devices cite: 17 (8 its own); citations of its devices by later devices: 10 (8 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
- Ethicon Endo-Surgery, Inc.: 2 (https://510kreport.com/company/ethicon-endo-surgery)
- Neothermia Corp.: 1 (https://510kreport.com/company/neothermia)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Senorx, Inc.: 1 (https://510kreport.com/company/senorx)
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)
- Megadyne Medical Products, Inc.: 1 (https://510kreport.com/company/megadyne-medical-products)
- Sanarus Medical, Inc.: 1 (https://510kreport.com/company/sanarus-medical)
- Bip USA, Inc.: 1 (https://510kreport.com/company/bip-usa)

## Firms that cite its devices most
- Transmed7, LLC: 1 (https://510kreport.com/company/transmed7)
- Sontina Medical, LLC: 1 (https://510kreport.com/company/sontina-medical)

## Its most-cited devices
- K023601: Rubicor Encapsule Breast Biopsy Device, Model 30086 (2002), cited by 3
- K030049: Modification to Rubicor Encapsule Breast Biopsy Device, Model 30086 (2003), cited by 2
- K053151: Rubicor Magic Breast Biopsy Device (2005), cited by 2
- K020047: Rubicor Breast Biopsy Device (2002), cited by 1
- K052506: Rubicor Encapsule Breast Biopsy Device, Model 31108 (2005), cited by 1
- K071048: Rubicor Magic Breast Biopsy Device, Model 31537 (2007), cited by 1

## Recent decisions
- K071048: Rubicor Magic Breast Biopsy Device, Model 31537 (May 15, 2007)
- K070275: Flexible Loop Electrosurgical Electrode (Mar 9, 2007)
- K053151: Rubicor Magic Breast Biopsy Device (Nov 18, 2005)
- K052506: Rubicor Encapsule Breast Biopsy Device, Model 31108 (Oct 6, 2005)
- K032584: Rubicor Encapsule Breast Biopsy Device, Model 30629 (Sep 17, 2003)
- K030049: Modification to Rubicor Encapsule Breast Biopsy Device, Model 30086 (Jan 29, 2003)
- K023601: Rubicor Encapsule Breast Biopsy Device, Model 30086 (Nov 19, 2002)
- K020047: Rubicor Breast Biopsy Device (Apr 5, 2002)

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