# Alcon

- Location (FDA's records): Fort Worth, TX
- FDA decisions: 9 (1983–2008): 5 510(k) clearances and 4 original PMA approvals
- Names in FDA's records: Alcon (6); Alcon, Inc. (3)
- Product codes: HQL (3), LPN (3), HQC (1), LZU (1), LWL (1)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 11 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Alcon Laboratories: 2 (https://510kreport.com/company/alcon-laboratories)
- Storz Instrument Co.: 1 (https://510kreport.com/company/storz-instrument)
- Allergan, Inc.: 1 (https://510kreport.com/company/allergan)
- Synergetics, Inc.: 1 (https://510kreport.com/company/synergetics)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Oasis Medical, Inc.: 1 (https://510kreport.com/company/oasis-medical)

## Firms that cite its devices most
- Alcon Research, Ltd.: 6 (https://510kreport.com/company/alcon-research)
- Alcon Manufacturing, Ltd.: 1 (https://510kreport.com/company/alcon-manufacturing)
- Alcon Laboratories: 1 (https://510kreport.com/company/alcon-laboratories)

## Its most-cited devices
- K063583: Alcon Vision System (2008), cited by 7
- K071236: Alcon Multi-Purpose Solution (2007), cited by 1

## Recent decisions
- K063583: Alcon Vision System (May 9, 2008)
- K071236: Alcon Multi-Purpose Solution (Dec 12, 2007)
- K040231: Inteliport Occluding Device (Jul 13, 2004)
- K031193: Soft (Hydrophilic) Contact Lens Care Solution (Jul 3, 2003)
- K981574: Opti-Free Express Multi-Purpose Solution (Jul 6, 1998)
- P950008: Silikon 1000 (Sep 25, 1997)
- P820035: Optiflex Anterior Chamber Lenses (L1-L5) (Feb 28, 1986)
- P800049: Models 1S & 1P (Mar 31, 1983)

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