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United Hip System, U-Motion II PS Cup, Multi-Hole

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
United Hip System, U-Motion II PS Cup,Multi-Hole FDA UDI
Generic Name
Ceramic-on-polyethylene total hip prosthesis FDA UDI
Device Name
U-Motion II PS Cup, multi-hole, Ø72mm FDA UDI
Model / Reference
1306-3472 FDA UDI
Description
U-Motion II PS Cup, multi-hole, Ø72mm FDA UDI

Identifiers

Catalog Number
1306-3472 FDA UDI
Primary DI / UDI-DI
04712771503364 FDA UDI
510(k) Number
K172833 FDA UDI
FDA Product Code
LZO FDA UDI
KWY FDA UDI
LWJ FDA UDI
JDI FDA UDI
MEH FDA UDI
OQI FDA UDI
GMDN Term
Ceramic-on-polyethylene total hip prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3390 FDA UDI
888.3360 FDA UDI
888.3350 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

Dimensions & Sizes

Size
Outer Diameter — 72 Millimeter FDA UDI

Category: Ceramic-on-polyethylene total hip prosthesisCeramic-on-ceramic total hip prosthesis

United Hip System, U-Motion II PS Cup, Multi-Hole by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic-on-ceramic total hip prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6de52600-a79e-4a21-bec9-9b9b4f9b76a1 37 fields · synced May 30, 2026