Skip to content

Infinity™ Everlast™ 33681108

by Wright Medical Technology, Inc.

Ref 33681108

Infinity™ Everlast™ 33681108 is a device classified as Class IIb in the EU and Class II in the US made by Wright Medical Technology, Inc., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-00889797074360) and listed in FDA GUDID since 7 Jul 2020 (UDI-DI 00889797074360), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00889797074360 Basic UDI-DI 00889797074360UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889797074360 UDI-DI Date7 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00889797074360 registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 00889797074360 listed 7 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889797074360
  2. Registered EUDAMED B-00889797074360

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Infinity EUDAMED
Infinity™ Everlast™ GUDID
Generic name
Fixed-bearing total ankle prosthesis
Device name
INFINITY™ ADAPTIS™ Cross-linked Poly Insert Sz 1/1+ H: 8mm
Model / Ref / Catalog
33681108
Primary DI / UDI-DI
00889797074360
Basic UDI-DI
B-00889797074360
FDA product code
HSN
EMDN code
P09050703 Ankle prostheses fixed inserts
GMDN term
Fixed-bearing total ankle prosthesis
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3110
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Height — 8 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: Fixed-bearing total ankle prosthesis

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES, OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)