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Head Relief Drill Ao 110027747

by Biomet Orthopedics, Inc.

Ref 110027747

Head Relief Drill Ao 110027747 is a device classified as Class IIa in the EU and Class II in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI B-00887868138546), cleared under FDA 510(k) K142658 on 13 Nov 2014 and listed in FDA GUDID since 19 Dec 2018 (UDI-DI 00887868138546), active as of 7 Nov 2026. 2 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

None ongoing

2 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K142658

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/MDD EUDAMED NumberB-00887868138546 Basic UDI-DI 00887868138546UDI-DIDate23 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868138546 UDI-DI Date19 Dec 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK142658 Date13 Nov 2014DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00887868138546 registered 23 Oct 2026 Active
  • FDA 510(k) K142658 decided 13 Nov 2014 Active
  • FDA GUDID UDI-DI 00887868138546 listed 19 Dec 2018 Listed

Recalls

2 recalls · FDA

  • 2 recalls, same reason

    • Terminated Z-1302-2019 FDA Class II initiated 28 Mar 2019
    • Terminated Z-1303-2019 FDA Class II initiated 28 Mar 2019

    There is a potential of fracture, bending or shearing of the driver.

Timeline

5 dated events

  1. Cleared FDA 510(k) K142658
  2. Listed FDA GUDID 00887868138546
  3. Recall initiated FDA recalls Z-1302-2019
  4. Recall initiated FDA recalls Z-1303-2019
  5. Registered EUDAMED B-00887868138546

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  • Withdrawn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
Head Relief Drill Ao
Generic name
Fluted surgical drill bit, single-use, non-sterile
Device name
MFA_Forefoot FRS_Head Relief Drill Bit
Model / Ref / Catalog
110027747
Primary DI / UDI-DI
00887868138546
Basic UDI-DI
B-00887868138546
510(k) Number
FDA product code
HWC
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
GMDN term
Fluted surgical drill bit, single-use, non-sterile
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3040
EU registration type
Legacy device (under a directive)
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: Fluted surgical drill bit, single-use, non-sterile

Cleared under the same submission (K142658)

and 8 more cleared under K142658

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

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