# Aidera AB

- Location (FDA's records): Goteborg, SE
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: MRZ (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 3 (1 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
- Confidant, Inc.: 2 (https://510kreport.com/company/confidant)
- Medtronic Minimed: 1 (https://510kreport.com/company/medtronic-minimed)
- Intermed Advisors, Inc.: 1 (https://510kreport.com/company/intermed-advisors)
- Imetrikus, Inc.: 1 (https://510kreport.com/company/imetrikus)

## Firms that cite its devices most
- Lifescan, Inc.: 1 (https://510kreport.com/company/lifescan)
- Tandem Diabetes Care, Inc.: 1 (https://510kreport.com/company/tandem-diabetes-care)

## Its most-cited devices
- K101806: Aidera Diasend System (2010), cited by 2
- K083221: Aidera Diasend (2009), cited by 1

## Recent decisions
- K101806: Aidera Diasend System (Dec 7, 2010)
- K083221: Aidera Diasend (Feb 3, 2009)

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