# Bip USA, Inc.

- Location (FDA's records): Niagara Falls, NY
- FDA decisions: 7 (1993–2003): 7 510(k) clearances
- Product codes: GDF (2), KNW (2), MJG (1), FCG (1), MDM (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 6 (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)
- Biopsys Medical, Inc.: 1 (https://510kreport.com/company/biopsys-medical)
- Promex, Inc.: 1 (https://510kreport.com/company/promex)

## Firms that cite its devices most
- Triopsy Medical, Inc.: 2 (https://510kreport.com/company/triopsy-medical)
- Transmed7, LLC: 1 (https://510kreport.com/company/transmed7)
- M.D.L. S.R.L.: 1 (https://510kreport.com/company/mdl)
- Rubicor Medical, Inc.: 1 (https://510kreport.com/company/rubicor-medical)

## Its most-cited devices
- K024089: Vacuflash Biopsy System (2003), cited by 2
- K934371: Bip Multi Modification (1994), cited by 2
- K934370: Bip Biopsy Needle Modification (1994), cited by 1

## Recent decisions
- K024089: Vacuflash Biopsy System (Mar 11, 2003)
- K934371: Bip Multi Modification (Apr 28, 1994)
- K934370: Bip Biopsy Needle Modification (Mar 7, 1994)
- K935457: Localization Wire or Marker - Surgical (Feb 17, 1994)
- K925870: Spacer (May 19, 1993)
- K925875: Horizontal Needle Guide Attachment (Apr 6, 1993)
- K925874: Breast Stabilizer (Mar 16, 1993)

Source page: https://510kreport.com/company/bip-usa