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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 9 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | P6 | FDA UDI | Class I | Active |
| Midmark | 1531018-015 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G2N/S2 | FDA UDI | Class II | Active |
| Midmark | 9A386001-868 | FDA UDI | Class I | Active |
| Midmark | P22/G3 | FDA UDI | Class I | Active |
| Midmark | 153592-004 | FDA UDI | Class I | Active |
| Midmark | P32SC/CV5R | FDA UDI | Class I | Active |
| Midmark | QC3-01 | FDA UDI | Class I | Active |
| Midmark | 9A678001 | FDA UDI | Class I | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Unknown |
| Midmark | 9A394001-859 | FDA UDI | Class I | Active |
| Midmark | CV3 | FDA UDI | Class I | Active |
| Midmark | DCV8-G2A/H | FDA UDI | Class II | Active |
| Midmark | 9A394001-847 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7DE-W1Y/H | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSVP-04 | FDA UDI | Class II | Active |
| Midmark | 9A382001-869 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2A/H | FDA UDI | Class II | Active |
| Midmark | P7015V | FDA UDI | Class II | Active |
| Ritter | 9A51001-860 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7DE-W2X/H | FDA UDI | Class II | Active |
| Midmark | P32SC/CV6 | FDA UDI | Class I | Active |
| Midmark ClearVision Digital Sensor System | XSDP-02 | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7-G1N | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-G0N/H/S2/L | FDA UDI | Class II | Active |
| Midmark | DCV8-G2A/H/SB | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSDS-06/L | FDA UDI | Class II | Active |
| Preva, 66" Reach, Export | PE7016 | FDA UDI | Class II | Active |
| Midmark | 9A739001-999 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5DE‐W2Y/H | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-G2N/S1 | FDA UDI | Class II | Active |
| Midmark | 9A179002-870 | FDA UDI | Class I | Active |
| Ritter | 253-015 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0A/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCD7-G2Z/SB | FDA UDI | Class II | Active |
| Ritter | 9A337001-851 | FDA UDI | Class I | Active |
| Midmark | P52SC/G6 | FDA UDI | Class I | Active |
| Midmark | P32-050 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W2Y/H/S1 | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSVP-06 | FDA UDI | Class II | Active |
| Midmark Digital Spirometer | 1-100-1235 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 9A628001 | FDA UDI | Class I | Active |
| Ritter | 9A51001-861 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0012 / 60-A0015 / 60-A1041 | FDA UDI | Class II | Active |
| Midmark | 153829-003 | FDA UDI | Class I | Unknown |
| Midmark | 9A378001-856 | FDA UDI | Class I | Active |
| Midmark | 029-5135-01 | FDA UDI | Class I | Active |
| Midmark | 029-7244-06 | 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. |