# Johnson & Johnson Surgical Vision, Inc.

- Location (FDA's records): Irvine
- FDA decisions: 11 (1983–2023): 4 510(k) clearances and 7 original PMA approvals
- Product codes: HQL (3), LZP (2), MFK (2), HQC (2), OOE (1), MSS (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 47 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Abbott Medical Optics, Inc.: 2 (https://510kreport.com/company/abbott-medical-optics)
- Sie Ag,Surgical Instrument Engineering: 1 (https://510kreport.com/company/sie-ag-surgical-instrument-engineering)
- Amo Manufacturing USA, LLC: 1 (https://510kreport.com/company/amo-manufacturing-usa)
- Duckworth & Kent, Ltd.: 1 (https://510kreport.com/company/duckworth-kent)

## Recent decisions
- K223566: ELITA™ Femtosecond Laser System, ELITA™ Patient Interface (Apr 14, 2023)
- K203060: VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control (Mar 12, 2021)
- K191949: UNFOLDER Vitan Inserter (Sep 13, 2019)
- K191933: COMPACT INTUITIV System, COMPACT INTUITIV Wireless Remote Control, COMPACT INTUITIV Four-Button Foot Pedal, COMPACT INTUITIV Closed-Toe Foot Pedal (Aug 16, 2019)
- P110007: Healon Endocoat Opviscosurgical Ophthalmic Device (Ovd) (3% Sodium Hyaluronate) (Jul 2, 2012)
- P080010: Tecnis Multifocal Foldable Posterior Chamber Intraocular Lens (Iol) (Jan 16, 2009)
- P990080: Ceeon Edge Foldable Ultraviolet Light-Absorbing Posterior Chamber Intraocular Lens, Model 911A (Apr 5, 2001)
- P980040: Sensar Soft Acrylic UV-Light Absorbing Posterior Chamber Intraocular Lens (Feb 3, 2000)

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