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SwissPlus® FMSM

by ZimVie US Corp LLC

Part of a family of 6 devices: see the family page

Ref FMSM

SwissPlus® FMSM is a device classified as Class IIb in the EU and Class I in the US made by ZimVie US Corp LLC, registered in EUDAMED on 28 Aug 2026 (Basic UDI-DI 844868F8HP) and listed in FDA GUDID since 10 Feb 2017 (UDI-DI 00889024014879), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number844868F8HP Basic UDI-DI 00889024014879UDI-DIDate28 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024014879 UDI-DI Date10 Feb 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 844868F8HP registered 28 Aug 2026 Active
  • FDA GUDID UDI-DI 00889024014879 listed 10 Feb 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889024014879
  2. Registered EUDAMED 844868F8HP

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Tapered SwissPlus® Abutment and Components EUDAMED
SwissPlus® GUDID
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Device name
Fixture Mount/Transfer
Model / reference
FMSM
Primary DI / UDI-DI
00889024014879
Basic UDI-DI
844868F8HP
FDA product code
NDP
EMDN code
P01020101 Dental implants
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class IIb EUDAMED
Class I GUDID
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class I

Device class is stated on each registry's own scale: Class IIb 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 implant suprastructure, temporary, preformed, single-use

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from ZimVie US Corp LLC

See all devices from ZimVie US Corp LLC →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Sutures
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)