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Nexcomp flow D2 9254

by Meta Biomed, Inc.

Model Nexcomp Flow D2

Nexcomp flow D2 9254 is a device classified as Class IIa in the EU and Class II in the US made by Meta Biomed, Inc., registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI B-08806387892540) and listed in FDA GUDID since 19 Sep 2016 (UDI-DI 08806387892540), active as of 25 Oct 2026.

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

CE MDD

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08806387892540 Basic UDI-DI 08806387892540UDI-DIDate14 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806387892540 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08806387892540 registered 14 Jul 2026 Active
  • FDA GUDID UDI-DI 08806387892540 listed 19 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08806387892540
  2. Registered EUDAMED B-08806387892540

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Nexcomp Flow EUDAMED
Nexcomp flow D2 GUDID
Generic name
Dental composite resin
Device name
Flowable Composite Resin
Model / reference
Nexcomp Flow D2 EUDAMED
9254 GUDID
Primary DI / UDI-DI
08806387892540
Basic UDI-DI
B-08806387892540
FDA product code
EBF
EMDN code
Q01010103 Dental restorative composites
GMDN term
Dental composite resin
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3690
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Nexcomp Flow D2
GUDID
9254
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

Device class is stated on each registry's own scale: Class IIa 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 composite resin

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from Meta Biomed, Inc.

See all devices from Meta Biomed, Inc. →

Properties

  • Implantable YesEUDAMEDNoGUDID
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (19, all answered No)