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Trident

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Trident FDA UDI
Generic Name
Polyethylene acetabulum prosthesis FDA UDI
Device Name
Constrained Acet. Liner FDA UDI
Model / Reference
690-10-28I FDA UDI
Description
Constrained Acet. Liner FDA UDI

Identifiers

Catalog Number
690-10-28I FDA UDI
Primary DI / UDI-DI
07613327024364 FDA UDI
PMA Number
P960047 FDA UDI
FDA Product Code
KWZ FDA UDI
GMDN Term
Polyethylene acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3310 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 28.0 Millimeter FDA UDI

Category: Polyethylene acetabulum prosthesis

Trident by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyethylene acetabulum 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 f8a9c730-c04a-4a14-85f1-78f209fc589e 36 fields · synced May 30, 2026