Tornier Perform® Reversed Glenoid

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name: Tornier Perform® Reversed Glenoid FDA UDI
Generic Name: Orthopaedic bone screw (non-sliding) FDA UDI
Device Name: Peripheral Screw FDA UDI
Model / Reference: DWJ322 FDA UDI
Description: Peripheral Screw FDA UDI

Identifiers

Catalog Number: DWJ322 FDA UDI
Primary DI / UDI-DI: 00846832090051 FDA UDI
FDA Product Code: KWS FDA UDI
PHX FDA UDI
GMDN Term: Orthopaedic bone screw (non-sliding) 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 5.0 Millimeter FDA UDI
Length — 22 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Tornier Perform® Reversed Glenoid by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

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Zavation — ZAVATION · Class II
STARDRIVE — Synthes GmbH · Class IIb
Arthrex® — Arthrex, Inc. · Class II
Cancellous Screw, Locking — I.T.S. GmbH · Class II
PANGEA — Stryker Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Tornier, Inc.

Sources (1)

FDA UDI 02250331-854e-4ba5-b8b9-fcdec44de12a 36 fields · synced May 31, 2026