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SynOcta Abutment

by Dentis Co., Ltd 8 variants

Ref DISOWA487N

SynOcta Abutment (DISOWA487N) is a Class IIb device made by Dentis Co., Ltd., registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI B-08800053078672), active as of 25 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800053078672 Basic UDI-DI 08800053078672UDI-DIDate8 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
DISOWA487N
Primary DI / UDI-DI
08800053078672
Basic UDI-DI
B-08800053078672
EMDN code
P01020101 Dental implants
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000012523
Authorised representative
BEST FIT IMPLANTS S.A. ES-AR-000048728

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from Dentis Co., Ltd.

See all devices from Dentis Co., Ltd. →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)