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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
DWJ722 FDA UDI
Description
Peripheral Screw FDA UDI

Identifiers

Catalog Number
DWJ722 FDA UDI
Primary DI / UDI-DI
00846832091232 FDA UDI
FDA Product Code
PHX FDA UDI
KWS 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

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

Dimensions & Sizes

Size
Length — 22 Millimeter FDA UDI
Outer Diameter — 5.0 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).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI 40b587c6-0e78-455d-a9eb-0c2c08b2b613 36 fields · synced May 30, 2026