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Midmark Progeny Imaging Software 45-A0023

by Midmark Corporation

Midmark Progeny Imaging Software 45-A0023 is a Class II device made by Midmark Corporation, cleared under FDA 510(k) K070664 on 26 Apr 2007, registered in EUDAMED and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00841709101380), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K070664

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00841709101380 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK070664 Date26 Apr 2007DecidedStatusActive
European UnionCE/MDR EUDAMED Number— Date—StatusActive

Official records

Across registries

3 registries list this device

  • FDA 510(k) K070664 decided 26 Apr 2007 Active
  • EUDAMED Active
  • FDA GUDID UDI-DI 00841709101380 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K070664
  2. Listed FDA GUDID 00841709101380

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Midmark Progeny Imaging Software
Generic name
General-purpose dental x-ray system application software
Model / Ref / Catalog
45-A0023
Primary DI / UDI-DI
00841709101380
510(k) Number
FDA product code
MUH
GMDN term
General-purpose dental x-ray system application software
Device class
Class II
Regulation number
872.1800
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose dental x-ray system application software

Cleared under the same submission (K070664)

and 1 more cleared under K070664

Similar devices in this category

Other devices filed under General-purpose dental x-ray system application software.

Other devices from Midmark Corporation

See all devices from Midmark Corporation →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)