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MK-dent PRIME LINE

by MK-Dent GmbH 3 variants

Ref LP54L

MK-dent PRIME LINE (LP54L) is a dental power tool handpiece motorless component (EU MDD Class IIa; FDA Class I; FDA product code EFB, Handpiece, Air-Powered, Dental) made by MK-Dent GmbH, registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI B-+E490LP54L1G), cleared under FDA 510(k) K051872 on 3 Oct 2005 and listed in FDA GUDID since 14 Oct 2024 (UDI-DI +E490LP54L1G), active as of 25 Oct 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 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K051872

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-+E490LP54L1G Basic UDI-DI +E490LP54L1GUDI-DIDate25 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number+E490LP54L1G UDI-DI Date14 Oct 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK051872 Date3 Oct 2005DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-+E490LP54L1G registered 25 Sep 2026 Active
  • FDA 510(k) K051872 decided 3 Oct 2005 Active
  • FDA GUDID UDI-DI +E490LP54L1G listed 14 Oct 2024 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K051872
  2. Listed FDA GUDID +E490LP54L1G
  3. Registered EUDAMED B-+E490LP54L1G

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  • Withdrawn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
Contra Angle Handpiece EUDAMED
MK-dent GUDID
Generic name
Dental power tool handpiece motorless component
Model / Ref / Catalog
LP54L, PRIME LINE
Primary DI / UDI-DI
+E490LP54L1G EUDAMED
E490LP54L1 GUDID
Basic UDI-DI
B-+E490LP54L1G
510(k) Number
FDA product code
EFB
EMDN code
Q010199 Conservative dentistry and endodontics devices - other
GMDN term
Dental power tool handpiece motorless component
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.4200
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
LP54L
GUDID
PRIME LINE
Primary DI / UDI-DIEUDAMED
+E490LP54L1G
GUDID
E490LP54L1
Device classEUDAMED
Class IIa
GUDID
Class I

The registries describe this device under different primary UDI-DIs (EUDAMED lists +E490LP54L1G; FDA GUDID lists E490LP54L1), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Dental power tool handpiece motorless component

Cleared under the same submission (K051872)

and 8 more cleared under K051872

Similar devices in this category

Other devices filed under CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER.

Other devices from MK-Dent GmbH

See all devices from MK-Dent GmbH →

Properties

  • Sterilise before use
  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (19, all answered No)