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Data / Medical devices / Surgical Eye Tray

Surgical Eye Tray (PZG): 18 FDA-registered makers in 6 countries

18 establishments in 6 countries are registered with the FDA to make Surgical Eye Tray (product code PZG, Class 1, 21 CFR 886.4350). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 1 recall event (0 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
PZG
Device class
1
Regulation
886.4350
Medical specialty
Ophthalmic

Makers by country

CountryMakers
United States10
China3
United Kingdom2
Mexico1
Belgium1
India1

Makers of Surgical Eye Tray

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
Anodyne SurgicalO Fallon, MO, United StatesManufacturer0000api.fda.gov
Alcon Research, LLCFort Worth, TX, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Alcon Research, LLCHouston, TX, United StatesManufacturer0000api.fda.gov
Beaver-Visitec International, Inc.Waltham, MA, United StatesSpecification developer0010api.fda.gov
Beaver-Visitec International, LtdBIDFORD-ON-AVON Warwickshire, United KingdomManufacturer0000api.fda.gov
Blink Medical LTDSolihull, United KingdomManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Convertors de Mexico S. de R.L. de C.VCD.JUAREZ Chihuahua, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Gri Medical & Electronic Technology Co., Ltd.JIAXING Zhejiang, ChinaManufacturer0000api.fda.gov
Hasa OptixBrussels Brussels-Capital Region, BelgiumManufacturer0000api.fda.gov
Hubei Lanbin Medical Group Co., Ltd.Xiaogan City Hubei, ChinaManufacturer, Repackager or relabeler0000api.fda.gov
Katena Products, Inc.Parsippany, NJ, United StatesSpecification developer0000api.fda.gov
Katena Products, Inc.Randolph, NJ, United StatesSpecification developer0000api.fda.gov
Malosa Medical Instruments (Changshu) LimitedChangshu Jiangsu, ChinaContract manufacturer0000api.fda.gov
Microspecialties LLCMiddletown, CT, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Oasis Medical, Inc.Glendora, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Times Surgical Co.Jaipur Rajasthan, IndiaManufacturer0000api.fda.gov
Zien Medical Technologies LLCSalt Lake City, UT, United StatesManufacturer0000api.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.