Skip to content

Leforte System Bone Plate 242.20CD12

by Jeil Medical Corporation

Ref 242.20CD12

Leforte System Bone Plate 242.20CD12 is a device classified as Class IIb in the EU and Class II in the US made by Jeil Medical Corporation, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI B-08806390801782), cleared under FDA 510(k) K150965 on 17 Sep 2015 and listed in FDA GUDID since 23 Nov 2015 (UDI-DI 08806390801782), active as of 7 Nov 2026.

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 found

in data synced 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K150965

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-08806390801782 Basic UDI-DI 08806390801782UDI-DIDate28 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806390801782 UDI-DI Date23 Nov 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK150965 Date17 Sep 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-08806390801782 registered 28 Oct 2026 Active
  • FDA 510(k) K150965 decided 17 Sep 2015 Active
  • FDA GUDID UDI-DI 08806390801782 listed 23 Nov 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K150965
  2. Listed FDA GUDID 08806390801782
  3. Registered EUDAMED B-08806390801782

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  • Withdrawn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
Leforte System EUDAMED
Leforte System Bone Plate GUDID
Generic name
Craniofacial fixation plate, non-bioabsorbable, non-customized
Model / reference
242.20CD12
Primary DI / UDI-DI
08806390801782
Basic UDI-DI
B-08806390801782
510(k) Number
FDA product code
JEY
EMDN code
P09120599 Bone fixation plates - other
GMDN term
Craniofacial fixation plate, non-bioabsorbable, non-customized
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
872.4760
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
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 fixation plate, non-bioabsorbable, non-customized

Cleared under the same submission (K150965)

and 8 more cleared under K150965

Similar devices in this category

Other devices filed under BONE FIXATION PLATES - OTHER.

Other devices from Jeil Medical Corporation

See all devices from Jeil Medical Corporation →

Properties

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