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Titan Reverse Shoulder System TMP-0960-01R

by Smith & Nephew, Inc.

Titan Reverse Shoulder System TMP-0960-01R is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 2 Feb 2023 (UDI-DI 00885556864593), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885556864593 UDI-DI Date2 Feb 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Titan Reverse Shoulder System
Generic name
Surgical implant template, reusable
Model / Ref / Catalog
TMP-0960-01R
Primary DI / UDI-DI
00885556864593
FDA product code
HWT
GMDN term
Surgical implant template, reusable
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical implant template, reusable

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)