Logical Dual Mobility CoCr Liner

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name: Logical Dual Mobility CoCr Liner FDA UDI
Generic Name: Metallic acetabular liner FDA UDI
Model / Reference: 01-042-01-0548 FDA UDI

Identifiers

Primary DI / UDI-DI: 09348215112417 FDA UDI
510(k) Number: K220495 FDA UDI
FDA Product Code: LZO FDA UDI
MEH FDA UDI
GMDN Term: Metallic acetabular liner FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3353 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

Yes

FDA UDI

Category: Metallic acetabular liner

Logical Dual Mobility CoCr Liner by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

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 II	Pending data

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Manufacturer

Manufacturer: Signature Orthopaedics Pty Ltd

Sources (1)

FDA UDI 9bdf4bdf-64c5-4a1e-8d5c-65c11cc1bfb3 33 fields · synced Jun 8, 2026