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Midmark Progeny Imaging Software

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark Progeny Imaging Software FDA UDI
Generic Name
General-purpose dental x-ray system application software FDA UDI
Device Name
X-ray system application software FDA UDI
Model / Reference
60-A0003 FDA UDI
Description
X-ray system application software FDA UDI

Identifiers

Catalog Number
60-A0003 FDA UDI
Primary DI / UDI-DI
00841709101397 FDA UDI
510(k) Number
K070664 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
General-purpose dental x-ray system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Midmark Progeny Imaging Software by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose dental x-ray system application software.

Cleared under the same submission

K070664 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 6a5c8ce3-8d03-4703-bd49-e3cca1c6ab35 36 fields · synced Jun 8, 2026