# Vitaphore Corp.

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 13 (1986–1992): 13 510(k) clearances
- Product codes: FOZ (2), KMK (2), LJS (2), MOE (2), KGX (2), FRO (1), HBA (1), JEC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Integra LifeSciences Corporation: 2 (https://510kreport.com/company/integra-lifesciences)
- Kendall: 2 (https://510kreport.com/company/kendall)
- Medex, Inc.: 1 (https://510kreport.com/company/medex)
- Westaim Technologies, Inc.: 1 (https://510kreport.com/company/westaim-technologies)

## Its most-cited devices
- K861563: Vitaguard Percutaneous Infection Control Kit (1986), cited by 2
- K914579: Silver Foam Wound Dressing (1992), cited by 1
- K895993: Vitapatch Antimicrobial Catheter Securement Device (1990), cited by 1
- K895920: Vitapatch Pin Protection Device for Percutaneous (1991), cited by 1
- K896455: Vitachoice Wound Dressing (1990), cited by 1

## Recent decisions
- K914579: Silver Foam Wound Dressing (Feb 21, 1992)
- K913148: Collagen Shield for Acute Care (Oct 15, 1991)
- K895920: Vitapatch Pin Protection Device for Percutaneous (Jun 6, 1991)
- K902558: Collagen Shield for Acute Care (Aug 17, 1990)
- K891993: Collagen Neurosponge (Mar 23, 1990)
- K896455: Vitachoice Wound Dressing (Feb 15, 1990)
- K895993: Vitapatch Antimicrobial Catheter Securement Device (Jan 11, 1990)
- K896046: Vitapatch Cath. Securement Device W/Chlorhexidine (Jan 11, 1990)

Source page: https://510kreport.com/company/vitaphore