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STERIZO Total Hip System

FDA UDI

Class II (US FDA UDI)

by CPM Medical Consultants, LLC

Identity

Trade Name
STERIZO Total Hip System FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
Taper Stem, Std Offset Sz 13.75 FDA UDI
Model / Reference
Rev A FDA UDI
Description
Taper Stem, Std Offset Sz 13.75 FDA UDI

Identifiers

Catalog Number
M-1100-1375 FDA UDI
Primary DI / UDI-DI
B565M110013751 FDA UDI
510(k) Number
K143314 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 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

Category: Coated femoral stem prosthesis, modularCeramic-on-polyethylene total hip prosthesis

STERIZO Total Hip System by CPM Medical Consultants, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic-on-polyethylene total hip 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 8144f23f-67ea-4961-a7f0-21de8711b423 36 fields · synced May 30, 2026