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Midmark Corporation

United States·US-MF-000002581

Last updated September 17, 2026

About

Midmark is a global manufacturer and supplier of healthcare products, equipment and diagnostic software for medical, veterinary, and dental markets.

From the manufacturer's own website. Source

Information

Country
United States
Address
60, Vista Drive, Versailles, United States
Phone
—
PRRC Contact
Adam Clutter
EUDAMED SRN
US-MF-000002581
FDA FEI Number
1523530
DUNS Number
—

Catalogue (1527)

Page 26 of 31
DeviceModel / ReferenceRegistriesClassStatus
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD6-W2Z/H
FDA UDI
Class IIActive
Midmark P22SC/P3
FDA UDI
Class IActive
Midmark 9A179002-860
EUDAMEDFDA UDI
Class IActive
Midmark 9A378001-858
FDA UDI
Class IActive
Midmark 153901-008
FDA UDI
Class IActive
Midmark IQholter® Electrodes 2-100-0060
FDA UDI
Class IIActive
Midmark VETPRO IntraOral Dental X-ray System DCV8-G2A/H/S3
FDA UDI
Class IIActive
Ritter 9A51001-855
FDA UDI
Class IActive
Midmark 9A386001-843
FDA UDI
Class IActive
Midmark PREVA IntraOral Dental X-ray System DCD8DE-W2Y/H/SB
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCDM-W0A/H
FDA UDI
Class IIActive
Preva, 66" Reach, Uk PE7016-UK
FDA UDI
Class IIActive
Preva, 76" Reach, Gray W/Two Stud Mount, 12" Cone DPD7-G2P
FDA UDI
Class IIActive
IQstress Prep Kits 2-100-0095
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System 30-A2200
FDA UDI
Class IIActive
Midmark OptiMax Digital Sensor System XSDP-04
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD6-G1N/S2
FDA UDI
Class IIActive
Midmark Progeny Imaging Software 60-A0003
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD7-W2Z/H/S2
FDA UDI
Class IIActive
Preva, 82" Reach, Uk PE7018-UK
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD6DE-W2X/H/S1
FDA UDI
Class IIActive
Midmark IQecg® Digital ECG 1-100-1330
FDA UDI
Class IIActive
Midmark ClearVision Digital Sensor System XSDQ-02
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System 30-A2196
FDA UDI
Class IIActive
Midmark IQholter EX Digital Holter 4-000-0113
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System P7017GM/H
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCDM-W0Z/H/S2
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD5-W2M/H/SB
FDA UDI
Class IIActive
Midmark VETPRO IntraOral Dental X-ray System DCV5-G1A/H/SC
FDA UDI
Class IIActive
Midmark Intraoral Digital Sensor XSVQ-06
FDA UDI
Class IIActive
Preva 2.0, Retrofit Kit, White XSAR‐W0
FDA UDI
Class IIActive
Midmark Digital ECG 4-000-0080
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System 30-A2203
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD8DE-W2Y/H/S1
FDA UDI
Class IIActive
Midmark Intraoral Digital Sensor XSVN-08
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD6-W1B/S1
FDA UDI
Class IIActive
Midmark OptiMax Digital Sensor System XSVS-03/L
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System 30-A0013
FDA UDI
Class IIActive
Midmark Digital Spirometer w/Calibration Syringe 4-000-0028
FDA UDI
Class IIActive
Midmark True Definition Scanner 78-8150-2258-3
FDA UDI
Class IIActive
Midmark Intraoral Digital Sensor XSDQ-06
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD6DE-W1Y/H
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD8DE-W2Y/H
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD7DE-W2Y/H/SB
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System P7018-P
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD6DE-W2Y/H/S2
FDA UDI
Class IIActive
Control Unit, Vetpro Dc 30-A1041
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD5‐G1N/SB
FDA UDI
Class IIActive
Midmark True Definition Scanner 41-0001-6049-3
FDA UDI
Class IIActive
Midmark Intraoral Digital Sensor XSDP-06
FDA UDI
Class IIActive

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Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Mar 5, 2003Z-0704-03—terminated

The pressure relief valve may fail to open properly.