Atlas FDA

TECNIS SIMPLICITY™ Delivery System

FDA premarket approval P980040/S179 · decided 2025-12-16

Approval details

PMA number
P980040
Supplement
S179
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TECNIS SIMPLICITY™ Delivery System
Generic name
intraocular lens
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2025-11-21
Decision date
2025-12-16
Days to decision
25 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
an increase in the maximum aeration phase load size for degassing of TECNIS 1-Piece intraocular lenses (IOL) with TECNIS SIMPLICITY Delivery System sterilized by Ethylene Oxide at AMO Groningen

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510(k) clearances by this applicant

RecordFirmDate
ELITA™ Femtosecond Laser System, ELITA™ Patient Interface (K223566)Johnson & Johnson Surgical Vision, Inc.2023-04-14
VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control (K203060)Johnson & Johnson Surgical Vision, Inc.2021-03-12
UNFOLDER Vitan Inserter (K191949)Johnson & Johnson Surgical Vision, Inc.2019-09-13
COMPACT INTUITIV System, COMPACT INTUITIV Wireless Remote Control, COMPACT INTUITIV Four-Button Foot Pedal, COMPACT INTUITIV Closed-Toe Foot Pedal (K191933)Johnson & Johnson Surgical Vision, Inc.2019-08-16