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Perform™ Humeral System DWS4426

by Tornier, Inc.

Perform™ Humeral System DWS4426 is a Class II device made by Tornier, Inc., listed in FDA GUDID since 10 Nov 2020 (UDI-DI 00846832078318), 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 Number00846832078318 UDI-DI Date10 Nov 2020ListedStatusListed 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  • Withdrawn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
Perform™ Humeral System
Generic name
Polyethylene reverse shoulder prosthesis cup
Model / Ref / Catalog
DWS4426
Primary DI / UDI-DI
00846832078318
FDA product code
PAO
GMDN term
Polyethylene reverse shoulder prosthesis cup
Device class
Class II
Regulation number
888.3660
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Outer Diameter — 42 Millimeter

Related devices

Category: Polyethylene reverse shoulder prosthesis cup

Similar devices in this category

Other devices filed under Polyethylene reverse shoulder prosthesis cup.

Other devices from Tornier, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)