MobiliT Cup

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name: MobiliT Cup FDA UDI
Generic Name: Acetabular shell FDA UDI
Device Name: MobiliT Cementless spray titanium + HA acetabular cup – Dia. 58 FDA UDI
Model / Reference: HDM658 FDA UDI
Description: MobiliT Cementless spray titanium + HA acetabular cup – Dia. 58 FDA UDI

Identifiers

Catalog Number: HDM658 FDA UDI
Primary DI / UDI-DI: 05056139200922 FDA UDI
510(k) Number: K191831 FDA UDI
FDA Product Code: LZO FDA UDI
MEH FDA UDI
GMDN Term: Acetabular shell 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

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Acetabular shell

MobiliT Cup by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K191831 also covers:

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: Corin Ltd

Sources (1)

FDA UDI 6393a6ff-b036-41f4-b370-716dba425903 36 fields · synced May 31, 2026