# Naviswiss AG

- Location (FDA's records): Brugg, CH
- FDA decisions: 3 (2020–2023): 3 510(k) clearances
- Product codes: OLO (2), LLZ (1)
- 510(k) review time since 2016: median 151 days, against 90 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (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
- Intellijoint Surgical, Inc.: 2 (https://510kreport.com/company/intellijoint-surgical)
- Lexi Co., Ltd.: 1 (https://510kreport.com/company/lexi)

## Its most-cited devices
- K193094: Naviswiss Hip Navigation System (2020), cited by 1

## Recent decisions
- K223351: Naviswiss Knee (Jan 31, 2023)
- K211429: NAVIPLAN - CT Planning Software for Total Hip Replacement (Oct 5, 2021)
- K193094: Naviswiss Hip Navigation System (Jun 10, 2020)

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