# Omni-Tract Surgical, Div. Minn. Scientific, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (1992–2000): 4 510(k) clearances
- Product codes: GCJ (1), GAD (1), DWX (1), HRX (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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 whose devices it cites most
- Minnesota Scientific, Inc.: 3 (https://510kreport.com/company/minnesota-scientific)

## Firms that cite its devices most
- Geomed Medizin-Technik GmbH & Co.: 1 (https://510kreport.com/company/geomed-medizin-technik)
- Baitella AG: 1 (https://510kreport.com/company/baitella)

## Its most-cited devices
- K950214: Abdominal Wall Retractor (1995), cited by 2

## Recent decisions
- K001339: Mri Fastsystem Retractor System (May 17, 2000)
- K992583: Mass (Micro-Access Spine System) (Oct 29, 1999)
- K950214: Abdominal Wall Retractor (Feb 6, 1995)
- K913803: Intraluminal Artery Stripper (Apr 24, 1992)

Source page: https://510kreport.com/company/omni-tract-surgical-div-minn-scientific