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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 11 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 153592-002 | FDA UDI | Class I | Active |
| Midmark | 641-004 | FDA UDI | Class I | Active |
| Midmark | P7017VM | FDA UDI | Class II | Active |
| Midmark | 153758-004 | FDA UDI | Class I | Active |
| Midmark | 029-7245-05 | FDA UDI | Class I | Active |
| Midmark | 204 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark | 9A739001-860 | FDA UDI | Class I | Active |
| Ritter | 9A337001-864 | FDA UDI | Class I | Active |
| Midmark | 9A386001-863 | FDA UDI | Class I | Active |
| Ritter | M11-042 / 9A599001 | FDA UDI | Class II | Active |
| Midmark | P32/CV6R | FDA UDI | Class I | Active |
| Preva, 56" Reach, Deutsch W/Two Stud Mount, White | PE7015-D2-W | FDA UDI | Class II | Active |
| Midmark | G5-050 | FDA UDI | Class I | Active |
| Ritter | 9A337001-861 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7-W2A | FDA UDI | Class II | Active |
| Midmark | 1531018-013 | FDA UDI | Class I | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 1531017-008 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G1A/H/SC | FDA UDI | Class II | Active |
| Progeny ClearVision | XSDN-0B | FDA UDI | Class II | Active |
| Midmark | 9A378001-999 | FDA UDI | Class I | Active |
| Midmark | PM-4 | FDA UDI | Class I | Active |
| Midmark | 153800-013 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0A/H/S2 | FDA UDI | Class II | Active |
| Midmark | P72SC/CV10 | FDA UDI | Class I | Active |
| Midmark | 153914-002 | FDA UDI | Class I | Active |
| Midmark | 9A179002-868 | FDA UDI | Class I | Active |
| Progeny imaging Domestic | 500-427 | FDA UDI | Class II | Active |
| Midmark | DCV6-G1A/H | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A1031 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2A/H/S2 | FDA UDI | Class II | Active |
| Midmark | CBML | FDA UDI | Class I | Active |
| Midmark | 002-1530-00 | FDA UDI | Class I | Active |
| Midmark | 9A497001-999 | FDA UDI | Class I | Active |
| Midmark | 9A739001-865 | FDA UDI | Class I | Active |
| Midmark | 9A382001-866 | FDA UDI | Class I | Active |
| Midmark | 9A739001-858 | FDA UDI | Class I | Active |
| Midmark | 153963-003 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A1037 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2205 | FDA UDI | Class II | Active |
| Midmark | 9A378001-814 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W2Y/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV5-G2X/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A394001-862 | FDA UDI | Class I | Active |
| Midmark | 029-7245-07 | FDA UDI | Class I | Active |
| Midmark | 029-5144-00 | FDA UDI | Class I | Active |
| Midmark | 153901-003 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-05/L | FDA UDI | Class II | Active |
| Preva, 56" Reach, Gray W/Two Stud Mount, 12" Cone | DPD5-G2P | FDA UDI | Class II | Active |
| Midmark | 9A390001-857 | 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. |