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Sign in to claim this brandTEVA PHARMACEUTICALS USA, INC.
US
Last updated May 30, 2026
What TEVA PHARMACEUTICALS USA, INC. makes
TEVA PHARMACEUTICALS USA, INC. manufactures synovial fluid supplementation medium, specifically the device named SYNOJOINT.
The company's products are classified as Class III devices and are listed in the FDA Unique Device Identifier (UDI) registry. TEVA PHARMACEUTICALS USA, INC. is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does TEVA PHARMACEUTICALS USA, INC. manufacture?
TEVA PHARMACEUTICALS USA, INC. manufactures synovial fluid supplementation medium, specifically the device named SYNOJOINT, which is used for medical purposes.
Where is TEVA PHARMACEUTICALS USA, INC. based?
TEVA PHARMACEUTICALS USA, INC. is based in the United States, as indicated by the provided device data.
Which regulatory registries list TEVA PHARMACEUTICALS USA, INC.'s devices?
TEVA PHARMACEUTICALS USA, INC.'s devices are listed in the FDA Unique Device Identifier (UDI) registry, as specified in the device data.
How are TEVA PHARMACEUTICALS USA, INC.'s devices classified?
TEVA PHARMACEUTICALS USA, INC.'s devices, such as SYNOJOINT, are classified as Class III devices, which is the highest risk category, according to the provided information.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- tevapharm.com
- —
- —
- [email protected]
- Phone
- +1(888)838-2872
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 001627975
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Synojoynt | 57844-181 | FDA UDI | Class III | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Teva Pharmaceuticals USA, Inc. has one FDA recall record initiated on March 30, 2012, which remains in a terminated status. The recall was issued due to a lack of assurance of sterility.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 30, 2012 | Z-1437-2012 | — | terminated | Lack of assurance of sterility |