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Titan™ Reverse Shoulder System

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Titan™ Reverse Shoulder System FDA UDI
Generic Name
Resurfacing humeral head prosthesis FDA UDI
Device Name
The Titan Reverse Shoulder humeral poly liner is designed to achieve stability of the glenohumeral joint. FDA UDI
Model / Reference
LNR096000R FDA UDI
Description
The Titan Reverse Shoulder humeral poly liner is designed to achieve stability of the glenohumeral joint. FDA UDI

Identifiers

Catalog Number
LNR-0960-00R FDA UDI
Primary DI / UDI-DI
10381780121558 FDA UDI
510(k) Number
K130050 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Resurfacing humeral head 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resurfacing humeral head prosthesis

Titan™ Reverse Shoulder System by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resurfacing humeral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66ac9e1a-a9e6-4f34-a8bb-2f8ee3b9a8a7 38 fields · synced Jun 8, 2026