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Startflow 90750

by Danville Materials, LLC

Ref 90750

Startflow 90750 is a device classified as Class IIa in the EU and Class II in the US made by Danville Materials, LLC, registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 081659402D0363B) and listed in FDA GUDID since 22 Jun 2016 (UDI-DI 00816594020689), 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 Number081659402D0363B Basic UDI-DI 00816594020689UDI-DIDate29 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00816594020689 UDI-DI Date22 Jun 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081659402D0363B registered 29 Sep 2026 Active
  • FDA GUDID UDI-DI 00816594020689 listed 22 Jun 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00816594020689
  2. Registered EUDAMED 081659402D0363B

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  • Withdrawn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
Startflow
Generic name
Light-cured dental restorative composite resin
Device name
Startflow Composite
Model / Ref / Catalog
90750
Primary DI / UDI-DI
00816594020689
Basic UDI-DI
081659402D0363B
FDA product code
EBF
EMDN code
Q01010103 Dental restorative composites
GMDN term
Light-cured dental restorative composite resin
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3690
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
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: Light-cured dental restorative composite resin

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from Danville Materials, LLC

See all devices from Danville Materials, LLC →

Properties

  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)