# Techlab Inc., Corporate Research Center

- Location (FDA's records): Blacksburg, VA
- FDA decisions: 5 (2007–2012): 5 510(k) clearances
- Product codes: GMZ (2), DEG (1), NBT (1), MHI (1)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 1 (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
- Techlab, Inc.: 3 (https://510kreport.com/company/techlab)
- Meridian Diagnostics, Inc.: 3 (https://510kreport.com/company/meridian-diagnostics)
- Inova Diagnostics, Inc.: 2 (https://510kreport.com/company/inova-diagnostics)
- Meridian Bioscience, Inc.: 2 (https://510kreport.com/company/meridian-bioscience)
- Alexon - Trend, Inc.: 2 (https://510kreport.com/company/alexon-trend)

## Firms that cite its devices most
- Meridian Bioscience, Inc.: 1 (https://510kreport.com/company/meridian-bioscience)

## Its most-cited devices
- K121364: Shiga Toxin Quik Chek (2012), cited by 1

## Recent decisions
- K121364: Shiga Toxin Quik Chek (Oct 2, 2012)
- K121411: Shiga Toxin Chek (Oct 2, 2012)
- K103673: Giardia/ Cryptosporidium Quik Chek (Aug 18, 2011)
- K071712: Leuko EZ Vue (Dec 4, 2007)
- K071711: Asca-Chek (Nov 7, 2007)

Source page: https://510kreport.com/company/techlab-corporate-research-center