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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 13 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-G1N | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD8-W2A | FDA UDI | Class II | Active |
| Midmark | 002-1534-00 | FDA UDI | Class I | Active |
| Midmark | 255-027 | FDA UDI | Class I | Active |
| Midmark | M3-041 | FDA UDI | Class II | Active |
| Midmark | 9A500001-232 | FDA UDI | Class I | Active |
| Midmark | G3-050 | FDA UDI | Class I | Active |
| Ritter | 203-017 | FDA UDI | Class I | Active |
| Midmark | P72SC/G7 | FDA UDI | Class I | Active |
| Midmark | 9A386001-852 | FDA UDI | Class I | Active |
| Midmark | 153963-001 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone, w/Nellcor SPO2 | FDA UDI | Class II | Active |
| Midmark | 647-003 | FDA UDI | Class I | Active |
| Midmark | 9A390001-843 | FDA UDI | Class I | Active |
| Midmark | 9A179002-863 | FDA UDI | Class I | Active |
| Midmark | 9A386001-232 | FDA UDI | Class I | Active |
| Midmark | DCV5-G2X/H/SC | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7017-P | FDA UDI | Class II | Active |
| Midmark | 604 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5‐W1A | FDA UDI | Class II | Active |
| Midmark | 630-021 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2M/H/S1 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G1A/H/S3 | FDA UDI | Class II | Active |
| Midmark | P21/CV3R | FDA UDI | Class I | Active |
| Midmark | 9A386001-866 | FDA UDI | Class I | Active |
| Ritter | 9A337001-858 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G1N/S1 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSDS-03 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐G2N/S2 | FDA UDI | Class II | Active |
| Ritter | 9A337001-843 | FDA UDI | Class I | Active |
| Midmark | 9A179002-855 | FDA UDI | Class I | Active |
| Midmark | 9A386001-848 | FDA UDI | Class I | Active |
| Ritter | 224-001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐G1N/S2 | FDA UDI | Class II | Active |
| Midmark | 9A179002-999 | FDA UDI | Class I | Active |
| Midmark | P32/G3 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0A/H | FDA UDI | Class II | Active |
| Ritter | M9-042 | FDA UDI | Class II | Active |
| Midmark | P52/G5 | FDA UDI | Class I | Active |
| Ritter | 9A51001-857 | FDA UDI | Class I | Active |
| Midmark | 9A739001-862 | FDA UDI | Class I | Active |
| Ritter | 9A51001-813 | FDA UDI | Class I | Active |
| Preva German Mobile System, White | PE7017DM-W | FDA UDI | Class II | Active |
| Midmark | 9A382001-859 | FDA UDI | Class I | Active |
| Midmark | 9A394001-999 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5-W2M/H/S1 | FDA UDI | Class II | Active |
| Midmark | 029-3713-02 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSDN-03 | FDA UDI | Class II | Active |
| Midmark | 641-003 | FDA UDI | Class I | Active |
| Midmark | 9A390001-868 | 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. |