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CORE Shoulder System

FDA UDI

Class II (US FDA UDI)

by LinkBio Corp.

Identity

Trade Name
CORE Shoulder System FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
20mm Probe - Left FDA UDI
Model / Reference
87-9133/20L FDA UDI
Description
20mm Probe - Left FDA UDI

Identifiers

Primary DI / UDI-DI
00810022403136 FDA UDI
510(k) Number
K241470 FDA UDI
FDA Product Code
QHE FDA UDI
KWS FDA UDI
PHX FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, reusable

CORE Shoulder System by LinkBio Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LinkBio Corp.

Sources (1)

  • FDA UDI 28917223-9271-46a4-9fbb-642e1fd87b17 34 fields · synced May 30, 2026