# Genetic Laboratories, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 4 (1982–1985): 3 510(k) clearances and 1 original PMA approval
- Product codes: DXZ (2), MCI (1), FPX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Bio-Vascular, Inc.: 4 (https://510kreport.com/company/bio-vascular)
- Synovis Surgical Innovations: 2 (https://510kreport.com/company/synovis-surgical-innovations)
- Argentum International, LLC: 1 (https://510kreport.com/company/argentum-international)

## Its most-cited devices
- K842066: Peri-Guard Pericardial Patch (1985), cited by 4
- K821532: Periguard Pericardial Patch (1982), cited by 2
- K842621: Suture Strip (1984), cited by 1

## Recent decisions
- K842066: Peri-Guard Pericardial Patch (Dec 30, 1985)
- K842621: Suture Strip (Oct 25, 1984)
- K821532: Periguard Pericardial Patch (Aug 19, 1982)
- P800064: Bioflow (TM) (Mar 10, 1982)

Source page: https://510kreport.com/company/genetic-laboratories