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Tornier Perform® Anatomic Augmented Glenoid

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Tornier Perform® Anatomic Augmented Glenoid FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Device Name
Keeled Glenoid Augment FDA UDI
Model / Reference
DWK506RA15 FDA UDI
Description
Keeled Glenoid Augment FDA UDI

Identifiers

Catalog Number
DWK506RA15 FDA UDI
Primary DI / UDI-DI
00846832090761 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Coated shoulder humeral stem prosthesis 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
Angle — 15 degree FDA UDI

Category: Coated shoulder humeral stem prosthesis

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

Similar devices

Also classified as Coated shoulder humeral stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI 22957ee0-a93c-4d34-8564-fbad61e75eee 36 fields · synced Jun 8, 2026