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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 17 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 029-11477-02 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7-W2M/H | FDA UDI | Class II | Active |
| Midmark | 9A392001-999 | FDA UDI | Class I | Active |
| Midmark | DCD7-G1Z/S1 | FDA UDI | Class II | Active |
| Ritter | 9A328002 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2B/S2 | FDA UDI | N/A | Active |
| Ritter | 9A337001-860 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6DE-W1X/H | FDA UDI | Class II | Active |
| Midmark | 9A739001-844 | FDA UDI | Class I | Active |
| Midmark | 9A393001-999 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2B/S1 | FDA UDI | Class II | Active |
| Midmark | 9A394001-860 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G2A/H/SC | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2223 | FDA UDI | Class II | Active |
| Ritter M11 Ultraclave | M11-022R | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5DE‐W2X/H/S1 | FDA UDI | Class II | Active |
| Midmark | P21 | FDA UDI | Class I | Active |
| Midmark | 9A179002-846 | FDA UDI | Class I | Active |
| Ritter M3 UltraFast | M3-003 | FDA UDI | Class II | Active |
| Midmark | G6 | FDA UDI | Class I | Active |
| Midmark | 9A51001-999 | FDA UDI | Class I | Active |
| Midmark | 9A427001 | FDA UDI | Class I | Active |
| Midmark | P52/CV10 | FDA UDI | Class I | Active |
| Midmark | DPD5-G2Q | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2M/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A179002-864 | FDA UDI | Class I | Active |
| Midmark | 9A382001-845 | FDA UDI | Class I | Active |
| Midmark | 9A410002 | FDA UDI | Class I | Active |
| Ceph attachment with sensor | C6000 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2222 | FDA UDI | Class II | Active |
| Midmark | XSVS-01 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2X/H/S3 | FDA UDI | Class II | Active |
| Ritter | 9A337001-855 | FDA UDI | Class I | Active |
| Midmark | 9A512001-870 | FDA UDI | Class I | Active |
| Midmark | 153964-018 | FDA UDI | Class I | Active |
| Midmark | 9A390001-856 | FDA UDI | Class I | Active |
| Midmark | 153818-006 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDN-05 | FDA UDI | Class II | Active |
| Midmark | DCD5-G1Z | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD7-W2M/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-855 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDMDE-W0Y/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 9A179002-858 | FDA UDI | Class I | Active |
| Midmark | 029-11477-01 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-0D | FDA UDI | Class II | Active |
| Midmark | IQvitals Zone, w/Wireless | FDA UDI | Class II | Active |
| Midmark | 9A378001-854 | FDA UDI | Class I | Active |
| Preva, 76" Reach, Export With Two Stud Mount | PE7017-P | FDA UDI | Class II | Active |
| Midmark | 626-002 | 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. |