# Surgvision GmbH

- Location (FDA's records): Munich, DE
- FDA decisions: 3 (2022–2024): 3 510(k) clearances
- Product codes: IZI (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Visionsense, Ltd.: 1 (https://510kreport.com/company/visionsense)
- Novadaq Technologies Ulc. (Now A Part of Stryker): 1 (https://510kreport.com/company/novadaq-technologies-ulc-now-a-part-of-stryker)

## Its most-cited devices
- K222240: Explorer Air® II (2023), cited by 1
- K214097: Explorer Air II (2022), cited by 1

## Recent decisions
- K234090: EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004) (Mar 20, 2024)
- K222240: Explorer Air® II (Feb 28, 2023)
- K214097: Explorer Air II (Feb 25, 2022)

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