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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 2 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 029-4739-02 | FDA UDI | Class I | Active |
| Midmark | 153906-018 | FDA UDI | Class I | Unknown |
| Midmark | P52/CV6R | FDA UDI | Class I | Active |
| Ritter | 9A51001-867 | FDA UDI | Class I | Active |
| Midmark | 9A739001-813 | FDA UDI | Class I | Active |
| Midmark | P32 | FDA UDI | Class I | Active |
| Midmark | DCV5-G2X/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV5-G1X/H/S4 | FDA UDI | Class II | Active |
| Midmark | P7017V | FDA UDI | Class II | Active |
| Midmark | 9A410001 | FDA UDI | Class I | Active |
| Midmark | 9A81001-853 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W2Y/H/SB | FDA UDI | Class II | Active |
| Midmark | DCV5-G1X/H | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5‐G2N | FDA UDI | Class II | Active |
| Ritter | 230-004 | FDA UDI | Class I | Unknown |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 9A382001-857 | FDA UDI | Class I | Active |
| Midmark | DCD7-G1Z | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVS-04 | FDA UDI | Class II | Active |
| Midmark | 9A179002-849 | FDA UDI | Class I | Active |
| Midmark | 153829-002 | FDA UDI | Class I | Unknown |
| Midmark | 9A386001-844 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSDQ-04 | FDA UDI | Class II | Active |
| Midmark IQvitals® Device Kit with touchscreen - Blood Pressure and Temperature | 4-000-0500 | FDA UDI | Class II | Active |
| Midmark | 153818-002 | FDA UDI | Class I | Active |
| Ceph Attachmetnt without sensor | C4000 | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System with Laptop | XSDN-01/L | FDA UDI | Class II | Active |
| Midmark | 029-7244-07 | FDA UDI | Class I | Active |
| Midmark | 9A378001-847 | FDA UDI | Class I | Active |
| Midmark | 153829-005 | FDA UDI | Class I | Unknown |
| Midmark | DCV5-G2A/H | FDA UDI | Class II | Active |
| Midmark | 647-002 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-W1A | FDA UDI | Class II | Active |
| Midmark | 1531018-017 | FDA UDI | Class I | Active |
| Midmark | 9A179002-844 | FDA UDI | Class I | Active |
| Midmark | 9A394001-858 | FDA UDI | Class I | Active |
| Midmark | DCV5-G1X/H/SB | FDA UDI | Class II | Active |
| Midmark | 153818-004 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W1B/SB | FDA UDI | Class II | Active |
| Midmark | 9A378001-860 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD8-G2N | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W1Y/H/S1 | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSVQ-08 | FDA UDI | Class II | Active |
| Midmark | 9A390001-870 | FDA UDI | Class I | Active |
| Midmark | 9A394001-845 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-G0N/H/S1 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2B/SB | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7-W2Z/H | FDA UDI | Class II | Active |
| Midmark | 9A739001-845 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6DE-W2Y/H | FDA UDI | Class II | 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. |