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Data / Medical devices / Sponge, Ophthalmic / United States

FDA-registered makers of Sponge, Ophthalmic in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Sponge, Ophthalmic (product code HOZ). 11 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Sponge, Ophthalmic
Product code
HOZ
Country
United States

Makers of Sponge, Ophthalmic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beaver-Visitec International, Inc.Waltham, MA, United StatesManufacturer, Specification developer6December 27, 1993010api.fda.gov
Carwild Corp.New London, CT, United StatesContract manufacturer, Specification developer2December 21, 1999010api.fda.gov
Atlanta Healthcare ServicesLawrenceville, GA, United StatesManufacturer, Repackager or relabeler, Specification developer1July 15, 1994000api.fda.gov
Alcon Research, LLCSinking Spring, PA, United StatesManufacturer1November 2, 1989000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer1March 19, 1993010api.fda.gov
Hurricane MedicalBradenton, FL, United StatesManufacturer1May 10, 1999000api.fda.gov
Katena Products, Inc.Parsippany, NJ, United StatesSpecification developer1February 15, 1990000api.fda.gov
Katena Products, Inc.Randolph, NJ, United StatesManufacturer, Specification developer1February 15, 1990000api.fda.gov
Med-Logics, Inc.Athens, TX, United StatesManufacturer, Repackager or relabeler, Specification developer1August 18, 2000000api.fda.gov
Oasis Medical, Inc.Glendora, CA, United StatesComplaint file establishment, Specification developer1December 15, 2008000api.fda.gov
Oasis Medical, Inc.Glendora, CA, United StatesManufacturer, Repackager or relabeler1December 15, 2008000api.fda.gov
American Surgical Company, LLCBeverly, MA, United StatesManufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Eagle Labs, LLCSaint Paul, MN, United StatesContract manufacturer0000api.fda.gov
Isomedix Operations, Inc.Minneapolis, MN, United StatesManufacturer for export0000api.fda.gov
Medtronic Xomed, Inc.Mystic, CT, United StatesManufacturer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Summit Medical LLCSaint Paul, MN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, 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.