Data / Medical devices / United States / Ferring Pharmaceuticals Inc.
Ferring Pharmaceuticals Inc.: FDA-registered device maker in Parsippany, NJ, United States, 1 PMA approval
Ferring Pharmaceuticals Inc. is registered with the FDA (registration 2244564) in Parsippany, NJ, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated December 3, 2004. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2244564
- FEI number
- 1000119907
- Address
- 100 Interpace Pkwy, Parsippany, NJ, United States, 07054
- Owner or operator
- FERRING PHARMACEUTICALS INC. (2244564)
- Roles
- Specification developer
- First device listed
- August 26, 2004
- Registered through
- 2026
- Brand names listed
- EUFLEXXA
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Acid, Hyaluronic, Intraarticular | MOZ | 3 | Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| December 3, 2004 | P010029 | EUFLEXXA (1% SODIUM HYALURONATE) | MOZ | 40 | September 2, 2026 | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| April 16, 2010 | 55407 | Not yet classified | Terminated | Euflexxa (1% sodium hyaluronate). Pre-filled syringe, Rx only, 3 syringes per carton; Manufactured by Ferring Pharmaceuticals In, Parsippany, NJ 07054; Manufactured by Bio-Technology General (Israel Ltd. Be er Tuvia, Kir | Out of Specification results for molecular weight or viscosity through the established expiration date. | accessdata.fda.gov |
Compare with other makers
Updated September 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.