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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 20 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | IQvitals Zone, Wireless with Masimo SPO2 | FDA UDI | Class II | Active |
| Midmark | 9A390001-844 | FDA UDI | Class I | Active |
| Midmark | DCV7-G1X/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCV7-G1A/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 255-026 | FDA UDI | Class I | Active |
| Control Unit Asm., Preva 2.0 | 30-A1062 | FDA UDI | Class II | Active |
| Midmark | 9A382001-851 | FDA UDI | Class I | Active |
| Midmark | 9A382001-846 | FDA UDI | Class I | Active |
| Midmark | 9A410004 | FDA UDI | Class I | Active |
| Midmark | 9A378001-853 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2B/SB | FDA UDI | Class II | Active |
| Midmark | 1531017-004 | FDA UDI | Class I | Active |
| Midmark | DCV6-G1X/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A386001-864 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-W2B/SB | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5‐G1N | FDA UDI | Class II | Active |
| Midmark ClearVision Digital Sensor System | XSDQ-01 | FDA UDI | Class II | Active |
| Midmark | 9A179002-814 | FDA UDI | Class I | Active |
| Midmark | 153758-002 | FDA UDI | Class I | Active |
| Midmark | 9A394001-850 | FDA UDI | Class I | Active |
| Midmark | G7-050 | FDA UDI | Class I | Active |
| Midmark | DCD8-G2Z/S1 | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-W1B | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCDMDE-W0Y/H | FDA UDI | Class II | Active |
| Midmark | P5 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H | FDA UDI | Class II | Active |
| Midmark | IQvitals Zone, Non-Wireless | FDA UDI | Class II | Active |
| Midmark | DCD5-G1Z/S1 | FDA UDI | Class II | Active |
| Ritter | 225-003 | FDA UDI | Class I | Active |
| Midmark | 9A389001-999 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSVN-04 | FDA UDI | Class II | Active |
| Ritter | 9A337001-863 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2X/H | FDA UDI | Class II | Active |
| Midmark | 640-011 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSDS-6 | FDA UDI | Class II | Active |
| Midmark | DPD7-G1P | FDA UDI | Class II | Active |
| Midmark | PM-3 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCDM-W0Z/H | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5DE‐W1X/H | FDA UDI | Class II | Active |
| Midmark | 9A382001-814 | FDA UDI | Class I | Active |
| Midmark | 153904-002 | FDA UDI | Class I | Active |
| Midmark | 029-5153-00 | FDA UDI | Class I | Active |
| Midmark OptiMax Digital Sensor System | XSDP-03 | FDA UDI | Class II | Active |
| Midmark | DCV5-G1A/H/S2 | FDA UDI | Class II | Active |
| Midmark | DCV6-G1X/H/S2 | FDA UDI | Class II | Active |
| Midmark | DPD5-G2P | FDA UDI | Class II | Active |
| Pan and Ceph system with one sensor, export | V5150C | FDA UDI | Class II | Active |
| Midmark | 9A390001-853 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A1026 | 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. |