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Initia Total Hip System

FDA UDI

Class II (US FDA UDI)

by Kyocera Corporation

Identity

Trade Name
Initia Total Hip System FDA UDI
Generic Name
Metal-on-polyethylene total hip prosthesis FDA UDI
Device Name
STDHO LINER 44-66/70 FDA UDI
Model / Reference
GMH02-200199 FDA UDI
Description
STDHO LINER 44-66/70 FDA UDI

Identifiers

Catalog Number
GMH02-200199 FDA UDI
Primary DI / UDI-DI
04547898307447 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Metal-on-polyethylene total hip prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metal-on-polyethylene total hip prosthesis

Initia Total Hip System by Kyocera Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metal-on-polyethylene total hip prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kyocera Corporation

Sources (1)

  • FDA UDI 0b29ad9a-23d5-49e7-9a94-693c68ee07e1 36 fields · synced May 30, 2026