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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 5 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 631-001 | FDA UDI | Class I | Active |
| M3 UltraFast | M3-002 | FDA UDI | Class II | Active |
| Midmark | 9A179002-232 | FDA UDI | Class I | Active |
| Midmark | 9A390001-849 | FDA UDI | Class I | Active |
| Midmark | 153964-011 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone, Non-Wireless with Masimo SPO2 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2X/H | FDA UDI | Class II | Active |
| Ritter | 9A51001-851 | FDA UDI | Class I | Active |
| Midmark | 9A82001-852 | FDA UDI | Class I | Active |
| Midmark | XSVS-02/L | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0016 | FDA UDI | Class II | Active |
| Midmark | 9A739001-869 | FDA UDI | Class I | Active |
| Midmark | 029-5507-00 | FDA UDI | Class I | Active |
| Ritter | 9A214002 | FDA UDI | Class I | Active |
| Midmark | 9A378001-864 | FDA UDI | Class I | Active |
| Ritter | 203-015 | FDA UDI | Class I | Active |
| Midmark | 9A378001-865 | FDA UDI | Class I | Active |
| Midmark | DCV6-G1A/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 153964-016 | FDA UDI | Class I | Active |
| Midmark | 255-023 | FDA UDI | Class I | Active |
| Midmark | 9A386001-854 | FDA UDI | Class I | Active |
| Midmark | 9A390001-866 | FDA UDI | Class I | Active |
| Midmark | 9A386001-853 | FDA UDI | Class I | Active |
| Midmark | P52/G6 | FDA UDI | Class I | Active |
| Ritter | 9A51001-814 | FDA UDI | Class I | Active |
| Midmark | 153964-013 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV7-G2A/H/SC | FDA UDI | Class II | Active |
| Ritter | 9A51001-869 | FDA UDI | Class I | Active |
| Midmark | 9A386001-857 | FDA UDI | Class I | Active |
| Midmark | 9A739001-847 | FDA UDI | Class I | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Active |
| Ritter | 9A337001-868 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G2N/SB | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV5-G1A/H/S4 | FDA UDI | Class II | Active |
| Midmark | P72SC/CV10R | FDA UDI | Class I | Active |
| Midmark | 153939-001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7016-P/H | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2198 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDMDE-W0Y/H/S1 | FDA UDI | Class II | Active |
| Ritter | 203-016 | FDA UDI | Class I | Active |
| Midmark | CV5 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone, w/Nellcor SPO2 and Wirless | FDA UDI | Class II | Active |
| Midmark | 9A179002-850 | FDA UDI | Class I | Active |
| Midmark | DCV7-G1X/H/S2 | FDA UDI | Class II | Active |
| Midmark | G10-050 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2228 | FDA UDI | Class II | Active |
| Midmark | DCV7-G2X/H/SC | FDA UDI | Class II | Active |
| Midmark | 153829-008 | FDA UDI | Class I | Unknown |
| Midmark | DPD7-G2P | 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. |