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Sign in to claim this brandMidmark 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
- Website
- www.midmark.com
- facebook.com/MidmarkCorporation
- [email protected]
- Phone
- —
- PRRC Contact
- Adam Clutter
- EUDAMED SRN
- US-MF-000002581
- FDA FEI Number
- 1523530
- DUNS Number
- —
Catalogue (1527)
Page 14 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 9A382001-856 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G1N/SB | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVS-03 | FDA UDI | Class II | Active |
| Midmark | 9A179002-867 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCVM-G0A/H/S4/L | FDA UDI | Class II | Active |
| Preva, 66" Reach, Deutsch W/Two Stud Mount, White | PE7016-D2-W | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System with Laptop | XSDS-02/L | FDA UDI | Class II | Active |
| Midmark | DCVM-G0A/H/SB | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSDP-05 | FDA UDI | Class II | Active |
| Ritter | 9A337001-845 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-G0N/H/S1/L | FDA UDI | Class II | Active |
| Midmark | P72-050 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W1B/SB | FDA UDI | Class II | Active |
| Midmark | DCD6-G2Z | FDA UDI | Class II | Active |
| Midmark | 9A179002-813 | FDA UDI | Class I | Active |
| Ritter | M9D-042 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2X/H/SB | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVP-03 | FDA UDI | Class II | Active |
| Midmark | 9A382001-868 | FDA UDI | Class I | Active |
| Midmark | 9A331001-232 | FDA UDI | Class I | Active |
| Midmark | 9A496001-232 | FDA UDI | Class I | Active |
| Midmark | 153740-004 | FDA UDI | Class I | Active |
| Ritter | 253-011 | FDA UDI | Class I | Active |
| Preva, 76" Reach, Deutsch W/Two Stud Mount, White | PE7017-D2-W | FDA UDI | Class II | Active |
| Midmark | 153915-002 | FDA UDI | Class I | Active |
| Midmark | 9A179002-857 | FDA UDI | Class I | Active |
| Ritter | 9A51001-862 | FDA UDI | Class I | Active |
| Midmark | 9A386001-850 | FDA UDI | Class I | Active |
| Midmark | P52/P5 | FDA UDI | Class I | Active |
| Midmark | 9A386001-855 | FDA UDI | Class I | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Unknown |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W1X/H/S2 | FDA UDI | Class II | Active |
| Ritter | 95-001-216 | FDA UDI | Class I | Unknown |
| Midmark Vantage Cephalometric Sensor | 60-A1004 | FDA UDI | Class II | Active |
| Midmark | 153592-006 | FDA UDI | Class I | Active |
| Ritter | 255-005 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0012 / 60-A1037 / 60-A1041 | FDA UDI | Class II | Active |
| Midmark | 9A179002-859 | FDA UDI | Class I | Active |
| Ritter | 9A51001-864 | FDA UDI | Class I | Active |
| Midmark | 9A390001-813 | FDA UDI | Class I | Active |
| Midmark | 029-7245-08 | FDA UDI | Class I | Active |
| Midmark | 9A378001-844 | FDA UDI | Class I | Active |
| Midmark | QC6-01 | FDA UDI | Class I | Active |
| Midmark | 1531017-001 | FDA UDI | Class I | Active |
| Midmark | DCD8-G2Z/S2 | FDA UDI | Class II | Active |
| Midmark | DCV5-G2X/H/SB | FDA UDI | Class II | Active |
| Midmark | P32SC/G5 | FDA UDI | Class I | Active |
| Midmark | 153963-002 | FDA UDI | Class I | Active |
| Midmark | 029-11477-00 | FDA UDI | Class I | Active |
| Midmark IQecg® Digital ECG | 4-000-0061 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
- CEpartner4U NL
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 5, 2003 | Z-0704-03 | — | terminated | The pressure relief valve may fail to open properly. |