← Back to catalogue

U1 Hip System, Bipolar Cup

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
U1 Hip System, Bipolar Cup FDA UDI
Generic Name
Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Device Name
U1 Bipolar cap,58mm FDA UDI
Model / Reference
1501-1058 FDA UDI
Description
U1 Bipolar cap,58mm FDA UDI

Identifiers

Catalog Number
1501-1058 FDA UDI
Primary DI / UDI-DI
04711605564830 FDA UDI
510(k) Number
K050269 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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 — 58 Millimeter FDA UDI

Category: Bipolar femoral head outer component, hemiarthroplasty

U1 Hip System, Bipolar Cup by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bipolar femoral head outer component, hemiarthroplasty.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b57ea7d7-d2d9-44d9-a490-4a4635ca9b4f 37 fields · synced May 30, 2026