FDA Review Panel · OP

FDA 510(k) Ophthalmic Devices

About Ophthalmic Devices

FDA 510(k) ophthalmic devices include diagnostic and surgical equipment for eye care. The FDA review panel code is OP.

Main categories:

  • Contact lenses - daily, extended wear, toric and multifocal lenses
  • Intraocular lenses (IOLs) - monofocal, toric and premium IOLs for cataract surgery
  • Ophthalmic lasers - excimer lasers for LASIK, Nd:YAG, photocoagulation
  • Retinal imaging systems - OCT, fundus cameras, fluorescein angiography
  • Diagnostic instruments - tonometers, perimeters, autorefractors, slit lamps

5094
Total
5076
Cleared
109d
Avg days
1976
Since

FDA 510(k) Cleared Ophthalmic Devices

This page lists all 5094 medical devices in the Ophthalmic specialty that have been submitted to the FDA through the 510(k) premarket notification process. Contact lenses, IOLs, ophthalmic lasers and retinal imaging systems.

  • 5076 devices cleared as substantially equivalent to a predicate device.
  • Average time to FDA decision: 109 days.
  • Records available from 1976 to the present.
  • Filter by product code using the sidebar to narrow results by device type.
150 Ophthalmic devices
1–12 of 150
Cleared Apr 30, 2026
FSYX Ocular Pressure Adjusting Pump
K252455 · Balance Ophthalmics, Inc.
QQJ · Applicator, Negative Pressure, External, Ocular · 268d
Cleared Apr 29, 2026
PUSCON WATER BALANCE-1DAY TINT (omafilcon A) SOFT (HYDROPHILIC) CONTACT LENS
K253885 · GEO MEDICAL CO., LTD.
LPL · Lenses, Soft Contact, Daily Wear · 146d
Cleared Apr 27, 2026
TearCare MGX System
K252409 · Sight Sciences, Inc.
ORZ · Eyelid Thermal Pulsation System · 269d
Cleared Apr 07, 2026
Voyager DSLT (430840610)
K252979 · Belkin Vision, Ltd.
HQF · Laser, Ophthalmic · 202d
Cleared Apr 01, 2026
RM Electrode (RMH 25-01)
K253586 · Retmap, Inc.
HLZ · Electrode, Corneal · 135d
Cleared Mar 27, 2026
GPA (hexafocon A) Rigid Gas Permeable Contact Lenses
K253822 · Zhuhai Fitlens Medical Technology Co., Ltd.
HQD · Lens, Contact (other Material) - Daily · 119d
Cleared Mar 25, 2026
Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)
K252052 · Bausch and Lomb, Incorporated
HQC · Unit, Phacofragmentation · 267d
Cleared Mar 19, 2026
Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens
K254269 · St. shine Optical Co., Ltd.
LPL · Lenses, Soft Contact, Daily Wear · 79d
Cleared Mar 18, 2026
VISUREF 600
K253834 · Carl Zeiss Vision GmbH
HJO · Biomicroscope, Slit-lamp, Ac-powered · 107d
Cleared Mar 13, 2026
Pegavision (Toufilcon B) Daily Disposable Soft (Hydrophilic) Contact Lenses
K252385 · Pegavision Corporation
LPL · Lenses, Soft Contact, Daily Wear · 225d
Cleared Mar 13, 2026
Pentacam® Cornea OCT
K251848 · Oculus Optikger?te GmbH
MXK · Device, Analysis, Anterior Segment · 270d
Cleared Feb 13, 2026
DAILIES TOTAL1®
K254052 · Alcon Laboratories, Inc.
LPL · Lenses, Soft Contact, Daily Wear · 58d

How to use this database

This page lists 5094 medical devices in the Ophthalmic specialty submitted to the FDA through the 510(k) premarket notification process. Of these, 5076 were cleared as substantially equivalent to a predicate device. Average FDA review time: 109 days. Records from 1976 to the present.

You can use this list to:

  • Find predicate devices for a new 510(k) submission
  • Verify the clearance status of a specific device
  • Identify FDA product codes related to ophthalmic
  • Compare similar cleared devices within this category
  • Research manufacturers active in this specialty

Each entry includes: device name, 510(k) number, product code, manufacturer and FDA decision date. Click any device to view the full submission details.

This information is based on publicly available FDA data and is intended for informational purposes only. It may not reflect current market or regulatory status. Always verify critical information at accessdata.fda.gov.

Looking for a specific ophthalmic device? Search by device name, K-number or manufacturer.

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