Data / Medical devices / Acid, Hyaluronic, Intraarticular
Acid, Hyaluronic, Intraarticular (MOZ): 13 FDA-registered makers in 6 countries
13 establishments in 6 countries are registered with the FDA to make Acid, Hyaluronic, Intraarticular (product code MOZ, Class 3). 9 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 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MOZ
- Device class
- 3
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| United States | 7 |
| Italy | 2 |
| Spain | 1 |
| Japan | 1 |
| Israel | 1 |
| Sweden | 1 |
Makers of Acid, Hyaluronic, Intraarticular
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.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fidia Farmaceutici SPA | ABANO TERME Padova, Italy | Manufacturer | 0 | 3 | 0 | 0 | api.fda.gov | |
| Anika Therapeutics, Inc. | Bedford, MA, United States | Manufacturer, Manufacturer for export | 0 | 2 | 0 | 0 | api.fda.gov | |
| Channel-Markers Medical LLC | Raleigh, NC, United States | Complaint file establishment, Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Meiji Pharma Spain | Alcala de Henares Madrid(Province), Spain | Complaint file establishment, Exporter to the US, Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Seikagaku Corporation, Takahagi Plant | TAKAHAGI-SHI Ibaraki, Japan | Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Bioventus LLC | Durham, NC, United States | Manufacturer, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ferring Pharmaceuticals Inc. | Parsippany, NJ, United States | Specification developer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Genzyme Corporation | Ridgefield, NJ, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| IBSA Farmaceutici Italia Srl | Lodi (San Grato) Lombardy, Italy | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Bio-Technology General (israel) Ltd. | KIRYAT MALACHI Southern, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifecore Biomedical LLC | Chaska, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Patheon Manufacturing Services LLC | Ridgefield, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Q-Med AB | Uppsala, Sweden | Contract manufacturer | 0 | 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.