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AnyOne Internal Fixture IF3513

by Megagen Implant Co. Ltd

Part of a family of 193 devices: see the family page

Ref IF3513C

AnyOne Internal Fixture IF3513 (IF3513C) 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 Jun 2026 (Basic UDI-DI 880972899208Q6), cleared under FDA 510(k) K123988 on 15 Aug 2013 and listed in FDA GUDID since 26 Jun 2015 (UDI-DI 08806388220663), 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) K123988

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 Number880972899208Q6 Basic UDI-DI 08806388220663UDI-DIDate24 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806388220663 UDI-DI Date26 Jun 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK123988 Date15 Aug 2013DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 880972899208Q6 registered 24 Jun 2026 Active
  • FDA 510(k) K123988 decided 15 Aug 2013 Active
  • FDA GUDID UDI-DI 08806388220663 listed 26 Jun 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K123988
  2. Listed FDA GUDID 08806388220663
  3. Registered EUDAMED 880972899208Q6

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  • Withdrawn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
AnyOne Internal Fixture
Generic name
Screw endosteal dental implant, two-piece
Model / Ref / Catalog
IF3513C, IF3513
Description
AnyOne Internal Ø3.5/ L=13
Primary DI / UDI-DI
08806388220663
Basic UDI-DI
880972899208Q6
510(k) Number
FDA product code
DZE
EMDN code
P01020101 Dental implants
GMDN term
Screw endosteal dental implant, two-piece
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
872.3640
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
IF3513C
GUDID
IF3513
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: Screw endosteal dental implant, two-piece

Cleared under the same submission (K123988)

and 8 more cleared under K123988

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

  • Supplied sterile
  • Single use
  • Implantable
  • Sutures
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)