# Luneau SA

- Location (FDA's records): Chartres Cedex, FR
- FDA decisions: 5 (1985–2017): 5 510(k) clearances
- Names in FDA's records: Luneau SA (3); Luneau Sas (2)
- Product codes: HKX (2), HJC (1), HJK (1), HKY (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 4 (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
- Sis Ltd., Surgical Instrument Systems: 1 (https://510kreport.com/company/sis-surgical-instrument-systems)
- Keeler Instruments, Inc.: 1 (https://510kreport.com/company/keeler-instruments)
- Oculus Optikgerate GmbH: 1 (https://510kreport.com/company/oculus-optikgerate)

## Firms that cite its devices most
- Sensor Medical Technology, LLC: 1 (https://510kreport.com/company/sensor-medical-technology)
- Oculus Optikgerate GmbH: 1 (https://510kreport.com/company/oculus-optikgerate)
- Luneau Technology Operations: 1 (https://510kreport.com/company/luneau-technology-operations)

## Its most-cited devices
- K143086: VX120 Ophthalmic Diagnostic Device (2015), cited by 2
- K162067: VX130 Ophthalmic Diagnostic Device (2017), cited by 1
- K023838: Luneau Sterile Tonometer Separation Prisms (2003), cited by 1

## Recent decisions
- K162067: VX130 Ophthalmic Diagnostic Device (Apr 24, 2017)
- K143086: VX120 Ophthalmic Diagnostic Device (Jun 1, 2015)
- K023838: Luneau Sterile Tonometer Separation Prisms (Feb 20, 2003)
- K022413: Luneau 3 Mirror Lens (Sep 24, 2002)
- K851557: Anesthesiometer (May 30, 1985)

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