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Reunion 5572-2800

by Stryker Corp.

Reunion 5572-2800 is a Class II device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2015 (UDI-DI 07613327098709), 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 Number07613327098709 UDI-DI Date24 Sep 2015ListedStatusListed 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  • Withdrawn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
Reunion
Generic name
Reverse shoulder prosthesis base plate
Model / Ref / Catalog
5572-2800
Primary DI / UDI-DI
07613327098709
FDA product code
KWS
GMDN term
Reverse shoulder prosthesis base plate
Device class
Class II
Regulation number
888.3660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Reverse shoulder prosthesis base plate

Similar devices in this category

Other devices filed under Reverse shoulder prosthesis base plate.

Other devices from Stryker Corp.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)