Trident

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name: Trident FDA UDI
Generic Name: Acetabular shell FDA UDI
Device Name: Hemispherical Acetabular Shell FDA UDI
Model / Reference: 502-01-56F FDA UDI
Description: Hemispherical Acetabular Shell FDA UDI

Identifiers

Catalog Number: 502-01-56F FDA UDI
Primary DI / UDI-DI: 07613153073109 FDA UDI
FDA Product Code: KWZ FDA UDI
KWL FDA UDI
MEH FDA UDI
KWY FDA UDI
MAY FDA UDI
JDI FDA UDI
LWJ FDA UDI
LPH FDA UDI
MBL FDA UDI
LZO FDA UDI
GMDN Term: Acetabular shell FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3310 FDA UDI
888.3360 FDA UDI
888.3353 FDA UDI
888.3390 FDA UDI
888.3350 FDA UDI
888.3358 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 56.0 Millimeter FDA UDI

Category: Acetabular shell

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

Similar devices

Also classified as Acetabular shell.

DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
Klassic HD Acetabular Cup with Ti-Coat — TOTAL JOINT ORTHOPEDICS, INC. · Class II
POLARCUP — Smith & Nephew, Inc. · Class II
ESOP® — FOURNITURES HOSPITALIERES INDUSTRIE · Class II
ESOP® — FOURNITURES HOSPITALIERES INDUSTRIE · Class II
InSitu Hip System — Nextstep Arthropedix · Class II
REFLECTION — Smith & Nephew, Inc. · Class II
Regenerex® Ringloc®+ Hip System — Biomet Orthopedics, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Howmedica Osteonics Corp.

Sources (1)

FDA UDI f9f07d49-562d-4149-9275-238349d185f1 35 fields · synced May 30, 2026