# Vision Rt, Ltd.

- Location (FDA's records): London, GB
- FDA decisions: 11 (2006–2026): 11 510(k) clearances
- Names in FDA's records: Vision Rt, Ltd. (8); Vision RT Limited (3)
- Product codes: IYE (11)
- 510(k) review time since 2016: median 99 days, against 103 for FDA's reviews in the same codes and years (3 of 8 faster)
- Predicates its devices cite: 14 (10 its own); citations of its devices by later devices: 16 (10 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Radformation, Inc.: 1 (https://510kreport.com/company/radformation)
- Varian Medical Systems, Inc.: 1 (https://510kreport.com/company/varian-medical-systems)
- Brainlab AG: 1 (https://510kreport.com/company/brainlab)
- Huestis Medical: 1 (https://510kreport.com/company/huestis-medical)

## Firms that cite its devices most
- C-Rad Positioning AB: 3 (https://510kreport.com/company/c-rad-positioning)
- Lap GmbH Laser Applikationen: 3 (https://510kreport.com/company/lap-laser-applikationen)

## Its most-cited devices
- K052682: Alignrt (2006), cited by 5
- K072171: Gatect-RT (2007), cited by 2
- K233622: AlignRT Plus (2024), cited by 2
- K212583: AlignRT Plus (2021), cited by 2
- K231185: MapRT (2023), cited by 1
- K203387: AlignRT Plus (2021), cited by 1

## Recent decisions
- K253012: AlignRT Plus (8.0) (Mar 18, 2026)
- K243301: MapRT (May 19, 2025)
- K233622: AlignRT Plus (Mar 29, 2024)
- K231185: MapRT (Jun 23, 2023)
- K212583: AlignRT Plus (Nov 10, 2021)
- K203387: AlignRT Plus (Mar 4, 2021)
- K193431: AlignRT Plus (Jan 3, 2020)
- K181218: AlignRT Plus (Aug 7, 2018)

Source page: https://510kreport.com/company/vision-rt