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Twin in Motion

by ModJaw

Ref TWIM

Twin in Motion (TWIM) is a jaw physiology evaluation system (EU MDR Class IIa; FDA Class I; FDA product code NFS, Device, Jaw Tracking, For Monitoring Jaw Positions) made by Modjaw, registered in EUDAMED on 7 Nov 2023 (Basic UDI-DI 3770022347TWIM3L) and listed in FDA GUDID since 3 Mar 2023 (UDI-DI 03770022347243), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3770022347TWIM3L Basic UDI-DI 03770022347243UDI-DIDate7 Nov 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number03770022347243 UDI-DI Date3 Mar 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 3770022347TWIM3L registered 7 Nov 2023 Active
  • FDA GUDID UDI-DI 03770022347243 listed 3 Mar 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03770022347243
  2. Registered EUDAMED 3770022347TWIM3L

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  • Withdrawn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

Generic name
Jaw physiology evaluation system
Model / Ref / Catalog
TWIM
Primary DI / UDI-DI
03770022347243 EUDAMED
03770022347212 GUDID
Basic UDI-DI
3770022347TWIM3L
FDA product code
NFS
EMDN code
Q0199 Odontology devices - other
GMDN term
Jaw physiology evaluation system
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.2060
Special device type
Software
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
03770022347243
GUDID
03770022347212
Device classEUDAMED
Class IIa
GUDID
Class I

The registries describe this device under different primary UDI-DIs (EUDAMED lists 03770022347243; FDA GUDID lists 03770022347212), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
FR-MF-000009804

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)