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Alliance® SBGL3703

by Zimmer, Inc.

Ref SBGL3703

Alliance® SBGL3703 is a device classified as Class IIa in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 889024AQL2V), cleared under FDA 510(k) K193180 on 24 Feb 2020 and listed in FDA GUDID since 28 Feb 2020 (UDI-DI 00889024575165), active as of 7 Nov 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K193180

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number889024AQL2V Basic UDI-DI 00889024575165UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024575165 UDI-DI Date28 Feb 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK193180 Date24 Feb 2020DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 889024AQL2V registered 30 Oct 2026 Active
  • FDA 510(k) K193180 decided 24 Feb 2020 Active
  • FDA GUDID UDI-DI 00889024575165 listed 28 Feb 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K193180
  2. Listed FDA GUDID 00889024575165
  3. Registered EUDAMED 889024AQL2V

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Alliance®
Generic name
Glenoid orthopaedic reamer
Device name
Alliance Glenoid Augment Reamer
Model / Ref / Catalog
SBGL3703
Primary DI / UDI-DI
00889024575165
Basic UDI-DI
889024AQL2V
Direct marketing DI
00889024575165
510(k) Number
FDA product code
KWS, KWT
EMDN code
L090999 Orthopaedic surgery cutting instruments, reusable - other
GMDN term
Glenoid orthopaedic reamer
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3660, 888.3650
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Glenoid orthopaedic reamer

Cleared under the same submission (K193180)

and 8 more cleared under K193180

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)