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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 3 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| M11 Horizontal Cassette Rack | 9A215001 | FDA UDI | Class II | Active |
| Midmark | M9-040 / 9A682001 | FDA UDI | Class II | Active |
| Midmark | P7016V | FDA UDI | Class II | Active |
| Midmark | 630-023 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | XSVS-01/L | FDA UDI | Class II | Active |
| Midmark | DCV6-G1A/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A390001-999 | FDA UDI | Class I | Active |
| Midmark | 9A739001-868 | FDA UDI | Class I | Active |
| Midmark | 9A406002 | FDA UDI | Class I | Active |
| Midmark | 153740-001 | FDA UDI | Class I | Active |
| Midmark | M9-041 / 9A682001 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVS-0C | FDA UDI | Class II | Active |
| Midmark | 002-1536-00 | FDA UDI | Class I | Active |
| Midmark | 9A739001-850 | FDA UDI | Class I | Active |
| Midmark | 029-7245-00 | FDA UDI | Class I | Active |
| Preva, 76" Reach, Export | PE7017 | FDA UDI | Class II | Active |
| Midmark | 153818-005 | FDA UDI | Class I | Active |
| Midmark | 626-003 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W1Y/H/S2 | FDA UDI | N/A | Active |
| Midmark | 9A390001-860 | FDA UDI | Class I | Active |
| Midmark | M11-041 / 9A599001 | FDA UDI | Class II | Active |
| Midmark | DPD6-G2P | FDA UDI | Class II | Active |
| Midmark | DCV5-G1A/H | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2B/S1 | FDA UDI | Class II | Active |
| Midmark IQspiro Digital Spirometer | 4-000-0025 | FDA UDI | Class II | Active |
| Midmark | 9A179002-865 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | P7015V-P | FDA UDI | Class II | Active |
| Midmark | P52/CV6 | FDA UDI | Class I | Active |
| SpeedClean | 002-0396-00 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVS-0C/L | FDA UDI | Class II | Active |
| Midmark | 9A386001-865 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2X/H/S4 | FDA UDI | Class II | Active |
| Midmark | 9A394001-863 | FDA UDI | Class I | Active |
| Midmark ClearVision Digital Sensor System | XSDS-01 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV5-G1A/H/S3 | FDA UDI | Class II | Active |
| Midmark | 9A390001-232 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-0D | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-G1N/SB | FDA UDI | Class II | Active |
| Ritter | 9A51001-868 | FDA UDI | Class I | Active |
| Midmark True Definition Scanner | 70-2014-0340-2 | FDA UDI | Class II | Active |
| Midmark | 9A382001-870 | FDA UDI | Class I | Active |
| Midmark ClearVision Digital Sensor System | XSDS-0B | FDA UDI | Class II | Active |
| Pan and ceph system with two sensors, export | V5100C | FDA UDI | Class II | Active |
| Midmark | M11-040R | FDA UDI | Class II | Active |
| Midmark | 153758-005 | FDA UDI | Class I | Active |
| Midmark | 9A401002 | FDA UDI | Class II | Active |
| Midmark | 9A179002-853 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | 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. |