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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 4 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 604 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W1B/S1 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV5-G2A/H/SC | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G2A/H/S4 | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0015 | FDA UDI | Class II | Active |
| Midmark IQholter® Digital Holter Recorder | 1-370-0005 | FDA UDI | Class II | Active |
| Midmark | P32SC/CV5 | FDA UDI | Class I | Active |
| Midmark | 153909-002 | FDA UDI | Class I | Active |
| Ritter | 9A51001-845 | FDA UDI | Class I | Active |
| Midmark | DCV5-G2X/H | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Ritter | 9A329003 | FDA UDI | Class I | Active |
| Midmark | 9A394001-864 | FDA UDI | Class I | Active |
| Midmark | 9A394001-865 | FDA UDI | Class I | Active |
| Midmark | 9A390001-850 | FDA UDI | Class I | Active |
| Midmark | 153829-007 | FDA UDI | Class I | Unknown |
| Midmark | 9A378001-232 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0B/H/SB | FDA UDI | Class II | Active |
| Midmark | DCV6-G1A/H/SB | FDA UDI | Class II | Active |
| Midmark | DCV8-G2X/H/SB | FDA UDI | Class II | Active |
| Midmark | M11-051 | FDA UDI | Class II | Active |
| Ritter | 203-018 | FDA UDI | Class I | Active |
| Midmark | 153964-015 | FDA UDI | Class I | Active |
| Midmark | 626-001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-G1N/S1 | FDA UDI | Class II | Active |
| Midmark | 9A411004 | FDA UDI | Class I | Active |
| Ritter | 9A337001-853 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCVM-G0A/H/S3 | FDA UDI | Class II | Active |
| Midmark | M9-050 | FDA UDI | Class II | Active |
| Midmark | 153906-017 | FDA UDI | Class I | Unknown |
| Midmark | P22-050 | FDA UDI | Class I | Active |
| Midmark | 9A394001-870 | FDA UDI | Class I | Active |
| Midmark | 9A394001-853 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7-G2N | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-G0N/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-852 | FDA UDI | Class I | Active |
| Midmark | 153963-007 | FDA UDI | Class I | Active |
| Midmark | 9A179002-848 | FDA UDI | Class I | Active |
| Control Unit Asm., Preva 2.0 Ral 9010 | 30-A1065 | FDA UDI | Class II | Active |
| Pan and Ceph system with one sensor | V5050C | FDA UDI | Class II | Active |
| Midmark | 153818-001 | FDA UDI | Class I | Active |
| Midmark | 153903-001 | FDA UDI | Class I | Active |
| Midmark | 9A390001-861 | FDA UDI | Class I | Active |
| Ritter | 9A51001-863 | FDA UDI | Class I | Active |
| Midmark | 9A395001-999 | FDA UDI | Class I | Active |
| Ritter | 230-003 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7DE-W1X/H/S2 | FDA UDI | Class II | Active |
| Ritter | 9A51001-859 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6DE-W2X/H | FDA UDI | Class II | Active |
| Midmark | 9A390001-859 | 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. |