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U2™ Hip

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
U2™ Hip FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
U2 XPE case FDA UDI
Model / Reference
9204-8020 FDA UDI
Description
U2 XPE case FDA UDI

Identifiers

Catalog Number
9204-8020 FDA UDI
Primary DI / UDI-DI
04719872177876 FDA UDI
510(k) Number
K110245 FDA UDI
K111546 FDA UDI
K122504 FDA UDI
K123550 FDA UDI
K132207 FDA UDI
FDA Product Code
JDI FDA UDI
LZO FDA UDI
KWY FDA UDI
LPH FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3353 FDA UDI
888.3390 FDA UDI
888.3358 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: Instrument tray, reusable

U2™ Hip by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, 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 aec8909d-b9ed-4264-a09d-78b7d67cb618 36 fields · synced May 30, 2026