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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 18 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | DCV6-G1X/H/SC | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD8-W2B | FDA UDI | Class II | Active |
| Ritter | M9D-042 / 9A599001 | FDA UDI | Class II | Active |
| Preva 2.0, Mobile Retrofit Kit | XSAM‐G0 | FDA UDI | Class II | Active |
| Midmark Progeny Imaging Software | 30-A0027 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2Z/H/S2 | FDA UDI | Class II | Active |
| Midmark | M9-040R | FDA UDI | Class II | Active |
| Midmark | 153758-003 | FDA UDI | Class I | Active |
| Midmark IQecg® Digital ECG | 1-100-1325 | FDA UDI | Class II | Active |
| M3 Printer | 9A401001 | FDA UDI | Class II | Active |
| Midmark | P72 | FDA UDI | Class I | Active |
| Midmark | 647-001 | FDA UDI | Class I | Active |
| Midmark | XSVN-02/L | FDA UDI | Class II | Active |
| Midmark | DCV7-G2X/H/S2 | FDA UDI | Class II | Active |
| Midmark | M9-040 | FDA UDI | Class II | Active |
| Midmark | TRML | FDA UDI | Class I | Active |
| Midmark | 029-7244-00 | FDA UDI | Class I | Active |
| Midmark | P52/CV10R | FDA UDI | Class I | Active |
| Midmark | 9A599001 | FDA UDI | Class II | Active |
| Midmark IQspiro® Digital Spirometer | 1-100-1225 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2Z/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV8-G2X/H/S3 | FDA UDI | Class II | Active |
| Pan system with ceph sensor | V5050 | FDA UDI | Class II | Active |
| Midmark | 1531017-003 | FDA UDI | Class I | Active |
| Midmark | 153963-005 | FDA UDI | Class I | Active |
| Ritter | M11-042 / 9A682001 | FDA UDI | Class I | Active |
| Midmark | P32SC/G3 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV7-G1A/H/S4 | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSVN-06 | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5-W2Z/H | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Ritter | 253-017 | FDA UDI | Class I | Active |
| Midmark | WAML | FDA UDI | Class I | Active |
| Midmark | 9A739001-867 | FDA UDI | Class I | Active |
| Ritter | 9A337001-870 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A2154 | FDA UDI | Class II | Active |
| Midmark | 9A390001-847 | FDA UDI | Class I | Active |
| Midmark | 029-4739-01 | FDA UDI | Class I | Active |
| Midmark | WAML | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5-W2Z/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A739001-866 | FDA UDI | Class I | Active |
| Midmark | DCV5-G1X/H/S1 | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-W2B | FDA UDI | Class II | Active |
| Ritter M3 UltraFast | M3-004 | FDA UDI | Class II | Active |
| Midmark | 9A394001-857 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSVQ-03 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2M/H/S2 | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System | XSDN-01 | FDA UDI | Class II | Active |
| Midmark | P32/P3 | FDA UDI | Class I | Active |
| Midmark | 153800-012 | FDA UDI | Class I | 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. |