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U1™ Hip

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
U1™ Hip FDA UDI
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Device Name
Cup trial, φ46mm FDA UDI
Model / Reference
1303-2046 FDA UDI
Description
Cup trial, φ46mm FDA UDI

Identifiers

Catalog Number
1303-2046 FDA UDI
Primary DI / UDI-DI
04719872167914 FDA UDI
510(k) Number
K110245 FDA UDI
K111546 FDA UDI
K122504 FDA UDI
K123550 FDA UDI
K132207 FDA UDI
FDA Product Code
LZO FDA UDI
KWY FDA UDI
LPH FDA UDI
JDI FDA UDI
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3390 FDA UDI
888.3358 FDA UDI
888.3350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabulum prosthesis trial, prefabricated, reusable

U1™ Hip by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabulum prosthesis trial, prefabricated, reusable.

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 14c8be4c-371c-482e-9c52-c128acb21bce 37 fields · synced Jun 8, 2026