Skip to the page

Data / Medical devices / Acid, Hyaluronic, Intraarticular / United States

FDA-registered makers of Acid, Hyaluronic, Intraarticular in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Acid, Hyaluronic, Intraarticular (product code MOZ). 5 have a 510(k) clearance or PMA approval on file and 1 has 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.

Device
Acid, Hyaluronic, Intraarticular
Product code
MOZ
Country
United States

Makers of Acid, Hyaluronic, Intraarticular in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anika Therapeutics, Inc.Bedford, MA, United StatesManufacturer, Manufacturer for export0200api.fda.gov
Channel-Markers Medical LLCRaleigh, NC, United StatesComplaint file establishment, Specification developer0200api.fda.gov
Bioventus LLCDurham, NC, United StatesManufacturer, Specification developer0100api.fda.gov
Ferring Pharmaceuticals Inc.Parsippany, NJ, United StatesSpecification developer0110api.fda.gov
Genzyme CorporationRidgefield, NJ, United StatesSpecification developer0100api.fda.gov
Lifecore Biomedical LLCChaska, MN, United StatesContract manufacturer0000api.fda.gov
Patheon Manufacturing Services LLCRidgefield, NJ, United StatesContract manufacturer0000api.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.