Euflexxa

FDA UDI

Class III (US FDA UDI)

by Ally Medical Supplies Ltd

Identity

Trade Name: Euflexxa FDA UDI
Generic Name: Synovial fluid supplementation medium FDA UDI
Model / Reference: None FDA UDI

Identifiers

Primary DI / UDI-DI: 05060459970045 FDA UDI
PMA Number: P010029 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

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

Euflexxa by Ally Medical Supplies Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

P010029 also covers:

Euflexxa — PAVAN TRADING LTD

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: Ally Medical Supplies Ltd

Sources (1)

FDA UDI e410db86-5bf8-41f1-8b5d-34f8b153cf53 34 fields · synced May 30, 2026