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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 15 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark PREVA IntraOral Dental X-ray System | P7015 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Ritter | 9A337001-814 | FDA UDI | Class I | Active |
| Midmark | 9A386001-860 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2Z/H/S1 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-G2N/S1 | FDA UDI | Class II | Active |
| Midmark | 9A427002 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7017-H | FDA UDI | Class II | Active |
| Midmark | 153592-001 | FDA UDI | Class I | Active |
| Midmark | 029-5153-02 | FDA UDI | Class I | Active |
| Ritter | 9A337001-813 | FDA UDI | Class I | Active |
| Midmark | P7 | FDA UDI | Class I | Active |
| Midmark | CEML-L | FDA UDI | Class I | Active |
| Midmark | 029-7244-05 | FDA UDI | Class I | Active |
| Midmark | 9A378001-870 | FDA UDI | Class I | Active |
| Midmark | DCDM-G0Z/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A378001-869 | FDA UDI | Class I | Active |
| Midmark | 1531018-012 | FDA UDI | Class I | Active |
| Midmark | XSVN-01 | FDA UDI | Class II | Active |
| Midmark | P32/CV6 | FDA UDI | Class I | Active |
| Midmark | DCV5-G1A/H/S1 | FDA UDI | Class II | Active |
| Midmark Progeny Vantage Digital Panoramic System with Cephalometric Sensor | 60-A1010 | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System | XSDN-02 | FDA UDI | Class II | Active |
| Midmark | 9A179002-861 | FDA UDI | Class I | Active |
| Midmark | 640-001 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-0D/L | FDA UDI | Class II | Active |
| Midmark | 9A386001-859 | FDA UDI | Class I | Active |
| Midmark | DCV6-G2A/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A378001-866 | FDA UDI | Class I | Active |
| Midmark | 153906-014 | FDA UDI | Class I | Unknown |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Ritter | 9A51001-870 | FDA UDI | Class I | Active |
| Midmark | G14-050 | FDA UDI | Class I | Active |
| Midmark | G7 | FDA UDI | Class I | Active |
| Midmark | 9A382001-862 | FDA UDI | Class I | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark | 9A82001-867 | FDA UDI | Class I | Active |
| Midmark | 9A378001-849 | FDA UDI | Class I | Active |
| Midmark | 153906-013 | FDA UDI | Class I | Unknown |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2Z/H/SB | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System | XSDP-01 | FDA UDI | Class II | Active |
| Midmark | M3-042 | FDA UDI | Class II | Active |
| Midmark | P52SC/CV10R | FDA UDI | Class I | Active |
| Midmark | 153964-017 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W2X/H/S2 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVN-04/L | FDA UDI | Class II | Active |
| Midmark | DCVM-G0A/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A386001-856 | FDA UDI | Class I | Active |
| Midmark | XSVS-02 | FDA UDI | Class II | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Unknown |
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. |