Synojoynt

FDA UDI

Class III (US FDA UDI)

by Teva Pharmaceuticals Usa, Inc.

Identity

Trade Name: SYNOJOYNT FDA UDI
Generic Name: Synovial fluid supplementation medium FDA UDI
Device Name: prefilled syringe FDA UDI
Model / Reference: 57844-181 FDA UDI
Description: prefilled syringe FDA UDI

Identifiers

Catalog Number: 57844-181 FDA UDI
Primary DI / UDI-DI: 00357844181137 FDA UDI
PMA Number: P170016 FDA UDI
FDA Product Code: MOZ FDA UDI
GMDN Term: Synovial fluid supplementation medium FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Synovial fluid supplementation medium

Synojoynt by Teva Pharmaceuticals Usa, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synovial fluid supplementation medium.

Euflexxa — ACRE PHARMA LIMITED · Class III
Gel-One® Cross-linked Hyaluronate — Seikagaku Corp. · Class III
Hymovis® High Molecular Weight Viscoelastic Hyaluronan, 24mg/3ml syringe, 1 pack — Fidia Farmaceutici · Class III
ORTHOVISC — SAIMA GLOBAL FARMA S.L. · Class III
Supartz — PAVAN TRADING LTD · Class III
Supartz — Arcera GmbH · Class III
VISCO-3 sodium hyaluronate — Seikagaku Corp. · Class III
Synvisc One (Synvisc Three) — PAVAN TRADING LTD · Class III

Cleared under the same submission

P170016 also covers:

Arthrex® — Arthrex, Inc.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Teva Pharmaceuticals Usa, Inc.

Sources (1)

FDA UDI c659f2e0-66cc-4069-a22a-ee869cc6f828 37 fields · synced Jun 8, 2026