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2.7mm System 99-9952

by Biomet Microfixation, Inc

Ref 99-9952

2.7mm System 99-9952 is a device classified as Class IIb in the EU and Class II in the US made by Biomet Microfixation, Inc, registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI B-00841036058579), cleared under FDA 510(k) K854886 on 21 Jan 1986 and listed in FDA GUDID since 17 Sep 2014 (UDI-DI 00841036058579), active as of 7 Nov 2026. One FDA recall is 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

1 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K854886

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-00841036058579 Basic UDI-DI 00841036058579UDI-DIDate23 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00841036058579 UDI-DI Date17 Sep 2014ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK854886 Date21 Jan 1986DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00841036058579 registered 23 Oct 2026 Active
  • FDA 510(k) K854886 decided 21 Jan 1986 Active
  • FDA GUDID UDI-DI 00841036058579 listed 17 Sep 2014 Listed

Recalls

1 recall · FDA

    • Terminated Z-0108-2011 FDA Unclassified (pre-2012) initiated 31 Aug 2010

    Mislabeled size: The 2.0/1.0 4 hole long plate, Lot 120150 is labeled as 01-9205 (2.0/1.0 4 Hole Long Plate), however, the package contains a 01-9204 (2.0/1.0 4 Hole Regular Plate).

Timeline

4 dated events

  1. Cleared FDA 510(k) K854886
  2. Recall initiated FDA recalls Z-0108-2011
  3. Listed FDA GUDID 00841036058579
  4. Registered EUDAMED B-00841036058579

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  • Withdrawn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
2.7mm System
Generic name
Craniofacial bone screw, non-bioabsorbable
Device name
Total Temporomandibular Joint(TMJ) Replacement System Screws
Model / Ref / Catalog
99-9952
Primary DI / UDI-DI
00841036058579
Basic UDI-DI
B-00841036058579
510(k) Number
FDA product code
JEY
EMDN code
P010103 Mandibular prostheses
GMDN term
Craniofacial bone screw, non-bioabsorbable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
872.4760
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 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: Craniofacial bone screw, non-bioabsorbable

Cleared under the same submission (K854886)

and 8 more cleared under K854886

Similar devices in this category

Other devices filed under MANDIBULAR PROSTHESES.

Other devices from Biomet Microfixation, Inc

See all devices from Biomet Microfixation, Inc →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)