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Angled Abutment MIAA3215E

by Megagen Implant Co. Ltd

Part of a family of 331 devices: see the family page

Ref MIAA3215ET

Angled Abutment MIAA3215E (MIAA3215ET) 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 24 Mar 2026 (Basic UDI-DI 880972899873H), cleared under FDA 510(k) K150537 on 21 Jul 2015 and listed in FDA GUDID since 27 Jul 2015 (UDI-DI 08806388226344), active as of 25 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 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K150537

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/MDR EUDAMED Number880972899873H Basic UDI-DI 08806388226344UDI-DIDate24 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806388226344 UDI-DI Date27 Jul 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK150537 Date21 Jul 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 880972899873H registered 24 Mar 2026 Active
  • FDA 510(k) K150537 decided 21 Jul 2015 Active
  • FDA GUDID UDI-DI 08806388226344 listed 27 Jul 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K150537
  2. Listed FDA GUDID 08806388226344
  3. Registered EUDAMED 880972899873H

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  • Withdrawn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
Angled Abutment
Generic name
Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog
MIAA3215ET, MIAA3215E
Primary DI / UDI-DI
08806388226344
Basic UDI-DI
880972899873H
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
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MIAA3215ET
GUDID
MIAA3215E
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 (K150537)

and 8 more cleared under K150537

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)