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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 24 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| M9 Ultraclave | M9-020R | FDA UDI | Class II | Active |
| Midmark | 9A179002-854 | FDA UDI | Class I | Active |
| Midmark | 9A386001-847 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7017 | FDA UDI | Class II | Active |
| Midmark | 9A390001-855 | FDA UDI | Class I | Active |
| Midmark | 9A378001-868 | FDA UDI | Class I | Active |
| Midmark | 153800-010 | FDA UDI | Class I | Active |
| Preva 2.0, Retrofit Kit | XSAR‐G0 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7016 | FDA UDI | Class II | Active |
| Ritter | 224-003 | FDA UDI | Class I | Active |
| Preva, 56" Reach, Export | PE7015 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐G2N/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-813 | FDA UDI | Class I | Active |
| Midmark | 9A386001-858 | FDA UDI | Class I | Active |
| Midmark | DCDM-G0Z/H | FDA UDI | Class II | Active |
| Midmark | 153639-001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2221 | FDA UDI | Class II | Active |
| Midmark | 9A382001-858 | FDA UDI | Class I | Active |
| Midmark | DCV7-G1A/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A512001-232 | FDA UDI | Class I | Active |
| Midmark | DCV6-G1X/H/S1 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSDS-0C | FDA UDI | Class II | Active |
| Midmark | 029-4857-00 | FDA UDI | Class I | Active |
| Midmark | 029-7244-03 | FDA UDI | Class I | Active |
| Ritter | M9D-042 / 9A682001 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5-W2Z/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A394001-856 | FDA UDI | Class I | Active |
| Midmark | 9A643001 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCVM-G0A/H/SC | FDA UDI | Class II | Active |
| Ritter | M9-042 / 9A682001 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSDN-0C | FDA UDI | Class II | Active |
| Preva, 82" Reach, Export With Two Stud Mount | PE7018-P | FDA UDI | Class II | Active |
| Ritter | 230-001 | FDA UDI | Class I | Active |
| Midmark | P22/CV3 | FDA UDI | Class I | Active |
| Midmark | M9-040 / 9A599001 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | DCV6-G1X/H/S4 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7DE-W2X/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A390001-814 | FDA UDI | Class I | Active |
| Midmark Vantage Cephalometric Sensor | 60-A1019 | FDA UDI | Class II | Active |
| Midmark | M11-040 / 9A682001 | FDA UDI | Class I | Active |
| Midmark IQvitals Device Kit w/touchscreen - Blood Pressure, Temperature and SpO2 | 4-000-0510 | FDA UDI | Class II | Active |
| Midmark | M11-040 / 9A599001 | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0012 / 60-A1037 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | XSVS-02/L | FDA UDI | Class II | Active |
| Midmark | DCVM-G0X/H/S2/L | FDA UDI | Class II | Active |
| Midmark | 153604LR | FDA UDI | Class I | Active |
| Midmark IQspiro® Digital Spirometer with Calibration Syringe | 4-000-0026 | FDA UDI | Class II | Active |
| Midmark | 646-001 | 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. |