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Titan™

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Titan™ FDA UDI
Generic Name
Reverse shoulder prosthesis base plate FDA UDI
Device Name
RSS Glenoid Baseplate-S FDA UDI
Model / Reference
GBP-0961-094-S FDA UDI
Description
RSS Glenoid Baseplate-S FDA UDI

Identifiers

Catalog Number
GBP-0961-094-S FDA UDI
Primary DI / UDI-DI
10381780467656 FDA UDI
510(k) Number
K181999 FDA UDI
FDA Product Code
PHX FDA UDI
GMDN Term
Reverse shoulder prosthesis base plate 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Reverse shoulder prosthesis base plate

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

Similar devices

Also classified as Reverse shoulder prosthesis base plate.

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 43dd0ddb-0e1e-458f-a415-c434e02dcfea 38 fields · synced May 30, 2026