# Andi Electromedical Aps

- Location (FDA's records): Carmel, IN
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: NHN (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (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
- Microlight Corporation of America: 1 (https://510kreport.com/company/microlight-of-america)

## Firms that cite its devices most
- Axiom Usa., Inc.: 1 (https://510kreport.com/company/axiom-usa)
- Powermedic Aps: 1 (https://510kreport.com/company/powermedic)
- Microlight Corporation of America: 1 (https://510kreport.com/company/microlight-of-america)

## Its most-cited devices
- K030692: Power Laser 90 (2003), cited by 3

## Recent decisions
- K030692: Power Laser 90 (Jul 17, 2003)

Source page: https://510kreport.com/company/andi-electromedical