# I.Z.I. Corp.

- Location (FDA's records): Owings Mills, MD
- FDA decisions: 7 (1992–2002): 7 510(k) clearances
- Product codes: IYE (2), KPQ (1), HAW (1), JAK (1), LNH (1), JAC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 26 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Klarity Medical & Equipment (GZ) Co., Ltd.: 1 (https://510kreport.com/company/klarity-medical-equipment-gz)
- I.Z.I. Medical Products Corp.: 1 (https://510kreport.com/company/izi-medical-products)
- Guidant Cardiac and Vascular Surgery: 1 (https://510kreport.com/company/guidant-cardiac-and-vascular-surgery)

## Its most-cited devices
- K022074: Spherz (2002), cited by 1
- K930752: CT/Mri Topographic Marker (1993), cited by 1
- K993742: Super Tissue (2000), cited by 1

## Recent decisions
- K022074: Spherz (Aug 13, 2002)
- K014022: Mri Line Marker (Mar 4, 2002)
- K003736: Mri Line Marker (Jan 18, 2001)
- K994117: MR Enhancer (Feb 4, 2000)
- K993742: Super Tissue (Feb 2, 2000)
- K930752: CT/Mri Topographic Marker (Nov 19, 1993)
- K922287: E.Z. Port (TM) Radiation Therapy Skin Markers (Oct 16, 1992)

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