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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 10 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 9A500001-858 | FDA UDI | Class I | Active |
| Midmark | 9A378001-861 | FDA UDI | Class I | Active |
| Midmark | 9A390001-848 | FDA UDI | Class I | Active |
| Midmark | 029-7244-02 | FDA UDI | Class I | Active |
| Midmark | 9A386001-869 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7015/H | FDA UDI | Class II | Active |
| Midmark | 153603LR | FDA UDI | Class I | Active |
| Midmark | 153641-001 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSVN-03 | FDA UDI | Class II | Active |
| M11 Ultraclave | M11-020R | FDA UDI | Class II | Active |
| Midmark | P52-050 | FDA UDI | Class I | Active |
| Midmark | P52SC/P6 | FDA UDI | Class I | Active |
| Midmark | 153829-004 | FDA UDI | Class I | Unknown |
| Midmark | 9A394001-866 | FDA UDI | Class I | Active |
| Midmark | 153656-001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G2N/S1 | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5-W2M/H | FDA UDI | Class II | Active |
| Midmark | DCV8-G2A/H/S1 | FDA UDI | Class II | Active |
| Midmark Digital Spirometer | 4-000-0027 | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A1038 | FDA UDI | Class II | Active |
| Midmark | P52 | FDA UDI | Class I | Active |
| Midmark | 1531017-005 | FDA UDI | Class I | Active |
| Midmark | 1531018-010 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0A/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A82001-232 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2Z/H/SB | FDA UDI | Class II | Active |
| Midmark | 626-006 | FDA UDI | Class I | Active |
| Ritter M9 Ultraclave | M9-022 | FDA UDI | Class II | Active |
| Midmark | 253-002 | FDA UDI | Class I | Active |
| Midmark | 9A179002-852 | FDA UDI | Class I | Active |
| Midmark | DCD6-G1Z/SB | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV7-G2A/H/S4 | FDA UDI | Class II | Active |
| Midmark | 1531017-002 | FDA UDI | Class I | Active |
| Midmark | 029-11701-00 | FDA UDI | Class I | Active |
| Disposable EZ-Trode ECG Electrodes | 2-100-0204 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2X/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV7-G1X/H/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐W1B/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-865 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2224 | FDA UDI | Class II | Active |
| Midmark | 9A382001-860 | FDA UDI | Class I | Active |
| Midmark | 9A739001-859 | FDA UDI | Class I | Active |
| Preva Export Mobile System | PE7017M | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2195 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 9A179002-847 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2Z/H/SB | FDA UDI | Class II | Active |
| Midmark | 255-022 | FDA UDI | Class I | Active |
| Midmark | P21-050 | FDA UDI | Class I | Active |
| Ritter | 9A337001-869 | 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. |