# Bioptron AG

- Location (FDA's records): Littleton, CO
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: NHN (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Tanses Technologies, Inc.: 1 (https://510kreport.com/company/tanses-technologies)

## Its most-cited devices
- K032216: Bioptron Pro Light Therapy System and Bioptron Compact Iii Light Therapy System (2004), cited by 1

## Recent decisions
- K032216: Bioptron Pro Light Therapy System and Bioptron Compact Iii Light Therapy System (Feb 4, 2004)

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