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Orthovisc

FDA UDI

Class III (US FDA UDI)

by Pavan Trading Ltd

Identity

Trade Name
Orthovisc FDA UDI
Generic Name
Synovial fluid supplementation medium FDA UDI
Device Name
Orthovisc is injected into the knee joint to cushion and lubricate. FDA UDI
Model / Reference
None FDA UDI
Description
Orthovisc is injected into the knee joint to cushion and lubricate. FDA UDI

Identifiers

Primary DI / UDI-DI
05060548950026 FDA UDI
PMA Number
P030019 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synovial fluid supplementation medium

Orthovisc by Pavan Trading Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synovial fluid supplementation medium.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pavan Trading Ltd

Sources (1)

  • FDA UDI f4fe8fe7-15f9-45ad-90e8-fb66674c6b0e 34 fields · synced Jun 1, 2026