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Data / Medical devices / Aid, Surgical, Viscoelastic

Aid, Surgical, Viscoelastic (LZP): 18 FDA-registered makers in 6 countries

18 establishments in 6 countries are registered with the FDA to make Aid, Surgical, Viscoelastic (product code LZP, Class 3, 21 CFR 886.4275). 8 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 10 recall events (1 Class I). 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 every maker of this deviceMakers in the United StatesWatch this device
Product code
LZP
Device class
3
Regulation
886.4275
Medical specialty
Ophthalmic

Makers by country

CountryMakers
United States13
Sweden1
Netherlands1
India1
Israel1
Belgium1

Makers of Aid, Surgical, Viscoelastic

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bausch & Lomb IncorporatedRochester, NY, United StatesComplaint file establishment, Specification developer0400api.fda.gov
Alcon Research, LLCFort Worth, TX, United StatesSpecification developer0300api.fda.gov
Johnson & Johnson Surgical Vision, Inc.Irvine, CA, United StatesManufacturer, Specification developer0210api.fda.gov
Amo Uppsala ABUppsala, SwedenManufacturer0100api.fda.gov
Anika Therapeutics, Inc.Bedford, MA, United StatesContract manufacturer, Manufacturer0120api.fda.gov
Bausch & Lomb IncorporatedClearwater, FL, United StatesManufacturer0100api.fda.gov
Nordic Pharma BVGSiriusdreef, NetherlandsSpecification developer0100api.fda.gov
Nordic Pharma, Inc.Berwyn, PA, United StatesSpecification developer0100api.fda.gov
AurolabMADURAI Tamil Nadu, IndiaManufacturer0000api.fda.gov
Bio-Technology General (israel) Ltd.KIRYAT MALACHI Southern, IsraelContract manufacturer0000api.fda.gov
Cima Technology, Inc.Pittsburgh, PA, United StatesManufacturer for export0000api.fda.gov
Eyekon Medical, Inc.Clearwater, FL, United StatesManufacturer for export0000api.fda.gov
Lifecore Biomedical LLCChaska, MN, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Novartis Manufacturing NVPuurs-Sint-Amands Antwerpen, BelgiumContract manufacturer0000api.fda.gov
Oasis Medical, Inc.Glendora, CA, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
U.S. Iol, Inc.Lexington, KY, United StatesManufacturer for export0000api.fda.gov
Visionary Medical Supplies, Inc.Madison, WI, United StatesManufacturer for export, Specification developer0000api.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.