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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 23 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | DCV8-G2X/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A179002-843 | FDA UDI | Class I | Active |
| Midmark | DCV8-G2X/H/SC | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W1X/H/S2 | FDA UDI | Class II | Active |
| Midmark | DCVM-G0X/H/S2 | FDA UDI | Class II | Active |
| Midmark | G5 | FDA UDI | Class I | Active |
| Midmark | M11-050 | FDA UDI | Class II | Active |
| Midmark | DCD5-G1Z/S2 | FDA UDI | Class II | Active |
| Midmark | DCV5-G2X/H/S4 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | CV6 | FDA UDI | Class I | Active |
| Midmark | DCV5-G2A/H/SB | FDA UDI | Class II | Active |
| Midmark | 153906-011 | FDA UDI | Class I | Unknown |
| Midmark PREVA IntraOral Dental X-ray System | P7016-P | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSDS-04 | FDA UDI | Class II | Active |
| Midmark | 9A739001-861 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2229 | FDA UDI | Class II | Active |
| Midmark | 9A382001-849 | FDA UDI | Class I | Active |
| Midmark | CEML | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W2Y/H/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-G1N/S2 | FDA UDI | Class II | Active |
| Midmark | 153901-006 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0012 / 60-A0016 | FDA UDI | Class II | Active |
| Midmark | 153964-014 | FDA UDI | Class I | Active |
| Midmark | P32/CV5R | FDA UDI | Class I | Active |
| Midmark | P72/G7 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H/S1 | FDA UDI | Class II | Active |
| Midmark | P21/CV3 | FDA UDI | Class I | Active |
| Midmark | 9A390001-864 | FDA UDI | Class I | Active |
| Midmark | 9A739001-814 | FDA UDI | Class I | Active |
| Midmark | 9A382001-850 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7017-P/H | FDA UDI | Class II | Active |
| Midmark | 153800-011 | FDA UDI | Class I | Active |
| Pan and Ceph system with two sensors | V5000C | FDA UDI | Class II | Active |
| Midmark | 9A378001-845 | FDA UDI | Class I | Active |
| Ritter | 9A51001-843 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2B/S2 | FDA UDI | Class II | Active |
| Midmark | 153603LR-E | FDA UDI | Class I | Active |
| M9/M11 Impact Dot Matrix Printer | 9A259001 | FDA UDI | Class II | Active |
| Midmark | DPD6-G2Q | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G1A/H/S4 | FDA UDI | Class II | Active |
| Midmark | 153818-003 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A1032 | FDA UDI | Class II | Active |
| Midmark | DCVM-G0A/H/S2/L | FDA UDI | Class II | Active |
| Midmark | DCV8-G2X/H/S4 | FDA UDI | Class II | Active |
| Midmark | IQvitals Zone, w/Masimo SPO2 and Wireless | FDA UDI | Class II | Active |
| Midmark | 9A394001-855 | FDA UDI | Class I | Active |
| Midmark | P32/CV5 | FDA UDI | Class I | Active |
| Midmark | 9A179002-862 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2Z/H/S2 | FDA UDI | N/A | 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. |