# Visus Health IT GmbH

- Location (FDA's records): Bochum, DE
- FDA decisions: 4 (2018–2023): 4 510(k) clearances
- Product codes: LLZ (4)
- 510(k) review time since 2016: median 76 days, against 116 for FDA's reviews in the same codes and years (4 of 4 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- Visus Technology Transfer GmbH: 1 (https://510kreport.com/company/visus-technology-transfer)

## Its most-cited devices
- K212321: JiveX (Model Number / Release: 5.3) (2021), cited by 1
- K181964: JiveX (2018), cited by 1
- K200703: JiveX (2020), cited by 1

## Recent decisions
- K231041: JiveX (Model Number / Release: 5.4) (Jul 14, 2023)
- K212321: JiveX (Model Number / Release: 5.3) (Sep 23, 2021)
- K200703: JiveX (Apr 14, 2020)
- K181964: JiveX (Oct 23, 2018)

Source page: https://510kreport.com/company/visus-health-it