# Avery Dennison Corporation

- Location (FDA's records): Mentor, OH
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: FRO (1)
- Predicates its devices cite: 1 (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
- Covalontechnologies, Inc.: 1 (https://510kreport.com/company/covalontechnologies)

## Firms that cite its devices most
- Solventum US, LLC: 1 (https://510kreport.com/company/solventum-us)

## Its most-cited devices
- K163529: ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) (2017), cited by 1

## Recent decisions
- K163529: ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) (Mar 29, 2017)

Source page: https://510kreport.com/company/avery-dennison