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Unity Total Knee System 123.072.00

by Corin Ltd

Ref 123.072.00Model Unity Total Knee instrument set

Unity Total Knee System 123.072.00 is a device classified as Class I in the EU and Class II in the US made by Corin Ltd, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI B-05055343881408), cleared under FDA 510(k) K113060 on 10 Sep 2012 and listed in FDA GUDID since 17 Aug 2016 (UDI-DI 05055343881408), active as of 23 Oct 2026. 3 FDA recalls are linked to it.

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

CE MDD 510(k)

Valid until

No date given

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

FDA recalls

2 ongoing

This device is named in the recall

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K113060

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05055343881408 Basic UDI-DI 05055343881408UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05055343881408 UDI-DI Date17 Aug 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK113060 Date10 Sep 2012DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-05055343881408 registered 15 Oct 2026 Active
  • FDA 510(k) K113060 decided 10 Sep 2012 Active
  • FDA GUDID UDI-DI 05055343881408 listed 17 Aug 2016 Listed

Recalls

3 recalls · 2 ongoing · FDA

  • 2 recalls, same reason

    • Ongoing Z-0213-2024 FDA Class II initiated 13 Oct 2023
    • Ongoing Z-0214-2024 FDA Class II initiated 13 Oct 2023

    Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa.

    • Terminated Z-0273-2023 FDA Class II initiated 31 Oct 2022

    The internal packaging system for devices may have damage to the blisters potentially damaging the device or compromising the sterility of the packaging.

Timeline

6 dated events

  1. Cleared FDA 510(k) K113060
  2. Listed FDA GUDID 05055343881408
  3. Recall initiated FDA recalls Z-0273-2023
  4. Recall initiated FDA recalls Z-0213-2024
  5. Recall initiated FDA recalls Z-0214-2024
  6. Registered EUDAMED B-05055343881408

Coverage

2 jurisdictions

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

Specification

EUDAMED · GUDID

Trade name
Tibia Baseplate Impactor EUDAMED
Unity Total Knee System GUDID
Generic name
Orthopaedic implant impactor, reusable
Model / Ref / Catalog
123.072.00, Unity Total Knee instrument set
Primary DI / UDI-DI
05055343881408
Basic UDI-DI
B-05055343881408
510(k) Number
FDA product code
JWH
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Orthopaedic implant impactor, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3560
EU registration type
Legacy device (under a directive)
EU market of registration
France
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 I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Orthopaedic implant impactor, reusable

Cleared under the same submission (K113060)

and 8 more cleared under K113060

Similar devices in this category

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

Other devices from Corin Ltd

See all devices from Corin Ltd →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)