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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 8 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ritter | 9A51001-852 | FDA UDI | Class I | Active |
| Midmark | 9A394001-861 | FDA UDI | Class I | Active |
| Midmark | DPD7-G2Q | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV6-G2A/H/S3 | FDA UDI | Class II | Active |
| Midmark | DCDM-G0Z/H/SB | FDA UDI | Class II | Active |
| Preva, 56" Reach Export W/Two Stud Mount | PE7015-P | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSDQ-05 | FDA UDI | Class II | Active |
| Ritter | 9A337001-847 | FDA UDI | Class I | Active |
| Midmark | 9A410006 | FDA UDI | Class I | Active |
| Midmark | 153839-003 | FDA UDI | Class I | Active |
| Midmark | 029-7245-03 | FDA UDI | Class I | Active |
| Midmark | 9A390001-852 | FDA UDI | Class I | Active |
| Midmark | 9A739001-854 | FDA UDI | Class I | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCVM-G0A/H/S4/L | FDA UDI | Class II | Active |
| Ritter | 9A337001-859 | FDA UDI | Class I | Active |
| Midmark | 9A411006 | FDA UDI | Class I | Active |
| Ritter | 9A337001-854 | FDA UDI | Class I | Active |
| Midmark | 9A739001-856 | FDA UDI | Class I | Active |
| Midmark | 9A179002-851 | FDA UDI | Class I | Active |
| Ritter | 9A51001-856 | FDA UDI | Class I | Active |
| Ritter | 9A214001 | FDA UDI | Class I | Active |
| Midmark | P32/G5 | FDA UDI | Class I | Active |
| Prep Kit - Midmark IQholter, 7-lead | 2-100-0090 | FDA UDI | Class II | Active |
| Midmark | 9A385001-999 | FDA UDI | Class I | Active |
| Midmark | 153964-010 | FDA UDI | Class I | Active |
| Midmark | P72/P7 | FDA UDI | Class I | Active |
| Midmark | 9A378001-857 | FDA UDI | Class I | Active |
| Midmark | 153964-012 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone, Wireless without SPO2 | FDA UDI | Class II | Active |
| Midmark | 641-010 | FDA UDI | Class I | Active |
| Midmark | 153906-012 | FDA UDI | Class I | Unknown |
| Midmark | 9A394001-867 | FDA UDI | Class I | Active |
| Midmark | P32SC/P5 | FDA UDI | Class I | Active |
| Midmark | 9A386001-870 | FDA UDI | Class I | Active |
| Midmark | 9A386001-861 | FDA UDI | Class I | Active |
| Midmark | 1531017-007 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2M/H/SB | FDA UDI | Class II | Active |
| Midmark | 9A382001-847 | FDA UDI | Class I | Active |
| Midmark | DPD7-G1Q | FDA UDI | Class II | Active |
| Midmark IQvitals® Device with touchscreen - Blood Pressure and Temperature | 1-100-1610 | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSVN-06/L | FDA UDI | Class II | Active |
| Midmark | 9A382001-848 | FDA UDI | Class I | Active |
| Midmark | 1531017-006 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2X/H/S3 | FDA UDI | Class II | Active |
| Midmark | P72SC/P10 | FDA UDI | Class I | Active |
| Midmark | DCD6-G1Z/S1 | FDA UDI | Class II | Active |
| Midmark | DCV7-G1A/H/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7018-P/H | FDA UDI | Class II | Active |
| Midmark | 029-7245-02 | FDA UDI | Class I | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A2116 | 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. |