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Trident

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Trident FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
0 Degree Polyethylene Insert FDA UDI
Model / Reference
621-00-22H FDA UDI
Description
0 Degree Polyethylene Insert FDA UDI

Identifiers

Catalog Number
621-00-22H FDA UDI
Primary DI / UDI-DI
07613327037302 FDA UDI
510(k) Number
K983382 FDA UDI
K983502 FDA UDI
FDA Product Code
MEH FDA UDI
LPH FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

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 — 22.0 Millimeter FDA UDI

Category: Non-constrained polyethylene acetabular liner

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

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

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 52ee6006-6c08-4687-9d6a-928381003acb 36 fields · synced May 30, 2026