Is this your brand? Sign in to claim ownership.
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 25 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 153758-001 | FDA UDI | Class I | Active |
| Midmark | 029-5111-00 | FDA UDI | Class I | Active |
| Midmark | DCV5-G1A/H/S2 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7DE-W1Y/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV5-G1X/H/S2 | FDA UDI | Class II | Active |
| Midmark | 255-021 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSVN-06/L | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W1Y/H/S2 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCVM-G0A/H/S4 | FDA UDI | Class II | Active |
| Midmark Vantage Cephalometric Sensor | 60-A1009 | FDA UDI | Class II | Active |
| Midmark | 1531018-018 | FDA UDI | Class I | Active |
| Midmark | 604 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark | 9A390001-869 | FDA UDI | Class I | Active |
| Midmark | 9A739001-843 | FDA UDI | Class I | Active |
| Midmark | 9A179002-866 | FDA UDI | Class I | Active |
| Midmark | CV5R | FDA UDI | Class I | Active |
| Midmark | DCD7-G2Z/S1 | FDA UDI | Class II | Active |
| Midmark | 029-7245-04 | FDA UDI | Class I | Active |
| Midmark Progeny Vantage Digital Panoramic System with Cephalometric Sensor | 60-A2009 | FDA UDI | Class II | Active |
| Midmark | DCD6-G2Z/S1 | FDA UDI | Class II | Active |
| Midmark | DCVM-G0A/H/S2/L | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSVS-08/L | FDA UDI | Class II | Active |
| Ritter | 9A51001-844 | FDA UDI | Class I | Active |
| Midmark | P10 | FDA UDI | Class I | Active |
| Midmark | 9A739001-870 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV5-G2A/H/S3 | FDA UDI | Class II | Active |
| Control Unit, Preva 2.0 Mobile Stand | 30-A1066 | FDA UDI | Class II | Active |
| Midmark | P52/P6 | FDA UDI | Class I | Active |
| Midmark | 255-024 | FDA UDI | Class I | Active |
| Pan system | V5000 | FDA UDI | Class II | Active |
| Midmark | 9A394001-854 | FDA UDI | Class I | Active |
| Ritter | 9A337001-866 | FDA UDI | Class I | Active |
| Midmark | 9A394001-844 | FDA UDI | Class I | Active |
| Midmark | DCV6-G1X/H | FDA UDI | Class II | Active |
| Ritter | 9A51001-232 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2A/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A739001-863 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H/SC | FDA UDI | Class II | Active |
| Midmark | 9A81001-232 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H/S4 | FDA UDI | Class II | Active |
| Midmark IQholter® Digital Holter Recorder Kit | 4-000-0119 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV8-G2A/H/S4 | FDA UDI | Class II | Active |
| Ritter | 9A329005 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7015-P/H | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 153603C | FDA UDI | Class I | Active |
| Midmark | 9A739001-851 | FDA UDI | Class I | Active |
| Midmark | 9A394001-813 | FDA UDI | Class I | Active |
| Midmark | DCDM-G0N/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-999 | 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. |