# Invitrogen Corporation

- Location (FDA's records): Grand Island
- FDA decisions: 2 (2002–2008): 1 510(k) clearance and 1 original PMA approval
- Product codes: NYQ (1), NDS (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Life Technologies Corporation: 1 (https://510kreport.com/company/life-technologies)

## Firms that cite its devices most
- Life Technologies Corporation: 2 (https://510kreport.com/company/life-technologies)
- Fujifilm Irvine Scientific: 1 (https://510kreport.com/company/fujifilm-irvine-scientific)
- Energy Delivery Solutions: 1 (https://510kreport.com/company/energy-delivery-solutions)

## Its most-cited devices
- K022086: Aim-V (R) Medium, Model 087-0112 (2002), cited by 4

## Recent decisions
- P050040: Spot-Light HER2 Cish Kit (Jul 1, 2008)
- K022086: Aim-V (R) Medium, Model 087-0112 (Dec 23, 2002)

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