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Tornier Perform Humeral System

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Tornier Perform Humeral System FDA UDI
Generic Name
Polyethylene reverse shoulder prosthesis cup FDA UDI
Device Name
VE 10° Reversed Insert, 65% FDA UDI
Model / Reference
DWX5366 FDA UDI
Description
VE 10° Reversed Insert, 65% FDA UDI

Identifiers

Catalog Number
DWX5366 FDA UDI
Primary DI / UDI-DI
00840338606648 FDA UDI
510(k) Number
K241878 FDA UDI
FDA Product Code
HSD FDA UDI
PHX FDA UDI
KWS FDA UDI
GMDN Term
Polyethylene reverse shoulder prosthesis cup FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 36 Millimeter FDA UDI

Category: Polyethylene reverse shoulder prosthesis cup

Tornier Perform Humeral System by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyethylene reverse shoulder prosthesis cup.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI a8cc13f3-a42e-4170-bbf1-5e2caa9257c0 37 fields · synced May 30, 2026