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Johnson & Johnson Surgical Vision, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories6
Latest FDA decision2026-07-28
TypeNumberDevice NameCodeDateActions
PMA P810031 AID, SURGICAL, VISCOELASTICLZP2026-07-28 View
PMA P980040 intraocular lensHQL2026-07-23 View
PMA P990080 intraocular lensHQL2026-06-03 View
PMA P080010 Lens, multifocal intraocularMFK2026-06-03 View
PMA P110007 AID, SURGICAL, VISCOELASTICLZP2025-01-15 View
PMA P880081 Unknown Device2024-09-27 View
510(k) K223566 ELITA™ Femtosecond Laser System, ELITA™ Patient InterfaceOOE2023-04-14 View
510(k) K203060 VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote ControlHQC2021-03-12 View
510(k) K191949 UNFOLDER Vitan InserterMSS2019-09-13 View
510(k) K191933 COMPACT INTUITIV System, COMPACT INTUITIV Wireless Remote Control, COMPACT INTUITIV Four-Button Foot Pedal, COMPACT INTUITIV Closed-Toe Foot PedalHQC2019-08-16 View
PMA P960028 Lens, multifocal intraocularMFK2017-10-27 View

Related Clinical Trials

NCT05574959Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens, Model DEN00VTERMINATEDNCT05575063Clinical Investigation of Healon EndoCoat Ophthalmic Viscosurgical Device (OVD)COMPLETEDNCT06250322A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular LensCOMPLETEDNCT06377514Clinical Investigation of the TECNIS® Next-Generation Intraocular LensCOMPLETED
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