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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 7 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark OptiMax Digital Sensor System | XSDQ-03 | FDA UDI | Class II | Active |
| Midmark | 153906-015 | FDA UDI | Class I | Unknown |
| Midmark | 253-001 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 153963-004 | FDA UDI | Class I | Active |
| Midmark | CV6R | FDA UDI | Class I | Active |
| Midmark | DCV5-G1X/H/S3 | FDA UDI | Class II | Active |
| Control Unit Asm., Preva | 30-A1025 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-G0N/H/S2 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W2Y/H/S2 | FDA UDI | Class II | Active |
| Midmark | 029-3713-01 | FDA UDI | Class I | Active |
| Midmark | 9A179002-845 | FDA UDI | Class I | Active |
| Midmark | 640-002 | FDA UDI | Class I | Active |
| Ritter | 255-003 | FDA UDI | Class I | Active |
| Midmark | 9A179002-869 | FDA UDI | Class I | Active |
| Midmark | DCD6-G2Z/SB | FDA UDI | Class II | Active |
| Midmark | 1531018-014 | FDA UDI | Class I | Active |
| Ritter | 9A337001-848 | FDA UDI | Class I | Active |
| Ritter | 9A337001-846 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0Z/H/S1 | FDA UDI | Class II | Active |
| Midmark | 253-003 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone, Wireless with Nellcor SPO2 | FDA UDI | Class II | Active |
| Ritter | 9A329006 | FDA UDI | Class I | Active |
| Midmark IQholter Digital Holter | 4-000-0110 | FDA UDI | Class II | Active |
| Midmark | 9A739001-853 | FDA UDI | Class I | Active |
| Midmark | 9A386001-867 | FDA UDI | Class I | Active |
| Ritter | 9A51001-849 | FDA UDI | Class I | Active |
| Control Unit Asm., Preva Export | 30-A1035 | FDA UDI | Class II | Active |
| Midmark | 641-005 | FDA UDI | Class I | Active |
| Ritter | 9A51001-858 | FDA UDI | Class I | Active |
| Midmark | 253-005 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2B/S2 | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System | XSDS-02 | FDA UDI | Class II | Active |
| Midmark | P32SC/P3 | FDA UDI | Class I | Active |
| Midmark | 153963-006 | FDA UDI | Class I | Active |
| Ritter | 9A337001-862 | FDA UDI | Class I | Active |
| Midmark | 9A512001-858 | FDA UDI | Class I | Active |
| Midmark | 9A179002-856 | FDA UDI | Class I | Active |
| Midmark | DCV6-G2A/H | FDA UDI | Class II | Active |
| Midmark | 9A394001-868 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-05 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7DE-W2Y/H/S2 | FDA UDI | Class II | Active |
| Midmark | P22SC/CV3 | FDA UDI | Class I | Active |
| Midmark | 153901-002 | FDA UDI | Class I | Active |
| Midmark | DCV8-G2A/H/S2 | FDA UDI | Class II | Active |
| Midmark | 029-7245-06 | FDA UDI | Class I | Active |
| Midmark Progeny Imaging Software | 60-A0007 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV7-G1A/H/S3 | FDA UDI | Class II | Active |
| Midmark | 9A382001-863 | 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. |