# Augmedit B.V.

- Location (FDA's records): Naarden, NL
- FDA decisions: 1 (2024–2024): 1 510(k) clearance
- Product codes: QIH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Apoqlar GmbH: 1 (https://510kreport.com/company/apoqlar)

## Recent decisions
- K240094: LumiNE US; Lumi (Sep 10, 2024)

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