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EZ Post AANEPH7057

by Megagen Implant Co. Ltd

Part of a family of 586 devices: see the family page

Ref AANEPH7057L

EZ Post AANEPH7057 (AANEPH7057L) is a device classified as Class IIb in the EU and Class II in the US made by Megagen Implant Co. Ltd, registered in EUDAMED on 5 Sep 2026 (Basic UDI-DI 880972899863F), cleared under FDA 510(k) K110955 on 22 Nov 2011 and listed in FDA GUDID since 23 Jun 2015 (UDI-DI 08806388201587), active as of 23 Oct 2026.

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

CE MDR 510(k)

Valid until

No date given

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

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K110955

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/MDR EUDAMED Number880972899863F Basic UDI-DI 08806388201587UDI-DIDate5 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806388201587 UDI-DI Date23 Jun 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK110955 Date22 Nov 2011DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 880972899863F registered 5 Sep 2026 Active
  • FDA 510(k) K110955 decided 22 Nov 2011 Active
  • FDA GUDID UDI-DI 08806388201587 listed 23 Jun 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K110955
  2. Listed FDA GUDID 08806388201587
  3. Registered EUDAMED 880972899863F

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
EZ Post
Generic name
Dental implant suprastructure, permanent, preformed
Device name
EZ Post Abutment
Model / Ref / Catalog
AANEPH7057L, AANEPH7057
Description
AnyRidge Internal Ø7/ C=5/ P=7/ Hex
Primary DI / UDI-DI
08806388201587
Basic UDI-DI
880972899863F
510(k) Number
FDA product code
NHA
EMDN code
P01020101 Dental implants
GMDN term
Dental implant suprastructure, permanent, preformed
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
872.3630
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
AANEPH7057L
GUDID
AANEPH7057
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: Dental implant suprastructure, permanent, preformed

Cleared under the same submission (K110955)

and 8 more cleared under K110955

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from Megagen Implant Co., Ltd.

See all devices from Megagen Implant Co., Ltd. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Sutures
  • Prescription use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (18, all answered No)