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Midmark Progeny Vantage Digital Panoramic System with Cephalometric Sensor

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark Progeny Vantage Digital Panoramic System with Cephalometric Sensor FDA UDI
Generic Name
Dental x-ray system collimator FDA UDI
Device Name
Panoramic X-ray PRIMARY COLLIMATOR Assembly FDA UDI
Model / Reference
60-A2009 FDA UDI
Description
Panoramic X-ray PRIMARY COLLIMATOR Assembly FDA UDI

Identifiers

Catalog Number
60-A2009 FDA UDI
Primary DI / UDI-DI
00841709102592 FDA UDI
510(k) Number
K122643 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Dental x-ray system collimator 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental x-ray system collimator

Midmark Progeny Vantage Digital Panoramic System with Cephalometric Sensor by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental x-ray system collimator.

Cleared under the same submission

K122643 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 03b9c39c-5451-4568-954f-b581602f1f30 37 fields · synced Jun 8, 2026