Midmark Progeny Imaging Software 30-A0027
Midmark Progeny Imaging Software 30-A0027 is a Class II device made by Midmark Corporation, cleared under FDA 510(k) K070664 on 26 Apr 2007 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00841709101373), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841709101373 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK070664 | Date26 Apr 2007 | StatusActive |
Official records
- AccessGUDID record 00841709101373
- FDA 510(k) database K070664
Across registries
- FDA 510(k) K070664 decided 26 Apr 2007 Active
- FDA GUDID UDI-DI 00841709101373 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K070664
- Listed FDA GUDID 00841709101373
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Midmark Progeny Imaging Software
- Generic name
- General-purpose dental x-ray system application software
- Model / Ref / Catalog
- 30-A0027
- Primary DI / UDI-DI
- 00841709101373
- 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
Similar devices in this category
Other devices filed under General-purpose dental x-ray system application software.