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Humelock II Cemented Shoulder System

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humelock II Cemented Shoulder System FDA UDI
Generic Name
Shoulder prosthesis screw FDA UDI
Device Name
HUMELOCK INSTRUMENT 2 PEGS GLENOID TRIAL SIZE XS FDA UDI
Model / Reference
926-1100 FDA UDI
Description
HUMELOCK INSTRUMENT 2 PEGS GLENOID TRIAL SIZE XS FDA UDI

Identifiers

Catalog Number
926-1100 FDA UDI
Primary DI / UDI-DI
03701037303313 FDA UDI
510(k) Number
K123814 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Shoulder prosthesis screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusableShoulder prosthesis screw

Humelock II Cemented Shoulder System by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder prosthesis screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI ef9ff439-5ca9-4397-9ba9-e887cb91bb24 36 fields · synced May 30, 2026