Data / Medical devices / Intraocular Lens / United States

FDA-registered makers of Intraocular Lens in the United States: 27 establishments

Name: FDA-registered makers of Intraocular Lens in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

27 establishments in the United States are registered with the FDA to make Intraocular Lens (product code HQL). 13 have a 510(k) clearance or PMA approval on file and 8 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in the United States Watch these makers

Device: Intraocular Lens
Product code: HQL
Country: United States

Makers of Intraocular Lens in the United States

Maker	Location	Role	PMA approvals	Recall events	Class I	Source
Bausch & Lomb Incorporated	Rochester, NY, United States	Complaint file establishment, Specification developer	6	2	0	api.fda.gov
Bausch & Lomb Incorporated	Clearwater, FL, United States	Manufacturer	5	7	1	api.fda.gov
Alcon Research, LLC	Huntington, WV, United States	Manufacturer	4	0	0	api.fda.gov
Alcon Research, LLC	Lesage, WV, United States	Manufacturer	4	0	0	api.fda.gov
Amo Puerto Rico Manufacturing, Inc	Anasco, PR, United States	Manufacturer	3	3	0	api.fda.gov
Johnson & Johnson Surgical Vision, Inc.	Irvine, CA, United States	Manufacturer, Specification developer	3	1	0	api.fda.gov
Bausch & Lomb Incorporated	Wilmington, MA, United States	Manufacturer	2	0	0	api.fda.gov
Staar Surgical Company	Monrovia, CA, United States	Complaint file establishment, Manufacturer	2	4	0	api.fda.gov
STAAR Surgical Company	Tustin, CA, United States	Specification developer	2	0	0	api.fda.gov
Alcon Research, LLC	Fort Worth, TX, United States	Specification developer	1	4	2	api.fda.gov
Carl Zeiss Meditec Production, LLC.	Ontario, CA, United States	Complaint file establishment, Manufacturer, Manufacturer for export	1	0	0	api.fda.gov
Eyekon Medical, Inc.	Clearwater, FL, United States	Contract manufacturer, Manufacturer, Manufacturer for export	1	0	0	api.fda.gov
Lenstec, Inc.	Saint Petersburg, FL, United States	Manufacturer	1	0	0	api.fda.gov
Aaren Scientific Inc	Rancho Cucamonga, CA, United States	Manufacturer for export	0	2	0	api.fda.gov
Advanced Vision Science, Inc.	Goleta, CA, United States	Manufacturer for export	0	0	0	api.fda.gov
Cima Technology, Inc.	Pittsburgh, PA, United States	Manufacturer for export	0	0	0	api.fda.gov
Ellis Ophthalmic Technologies, Inc	Jamaica, NY, United States	Manufacturer	0	0	0	api.fda.gov
Isomedix Operations Inc.	S Plainfield, NJ, United States	Contract sterilizer, Manufacturer for export	0	0	0	api.fda.gov
Isomedix Operations, Inc	Ontario, CA, United States	Manufacturer for export	0	0	0	api.fda.gov
Jellisee Ophthalmics Inc.	McLean, VA, United States	Manufacturer for export	0	0	0	api.fda.gov
Medennium, Inc.	Irvine, CA, United States	Manufacturer for export	0	0	0	api.fda.gov
Millennium Biomedical, Inc.	Pomona, CA, United States	Manufacturer for export	0	0	0	api.fda.gov
Ophthalmic Solution Inc.	Knoxville, TN, United States	Manufacturer for export	0	0	0	api.fda.gov
Sterilization Services Of Georgia, Inc.	Atlanta, GA, United States	Manufacturer for export	0	0	0	api.fda.gov
Tekia, Inc.	Irvine, CA, United States	Manufacturer for export	0	3	0	api.fda.gov
U.S. Iol, Inc.	Lexington, KY, United States	Manufacturer for export, Repackager or relabeler	0	0	0	api.fda.gov
Visionary Medical Supplies, Inc.	Madison, WI, United States	Manufacturer for export, Specification developer	0	0	0	api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.