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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
What Midmark Corporation makes
Midmark Corporation manufactures stationary intraoral digital dental X-ray systems, electric and examination dental chairs with reusable headrests, intraoral digital imaging sensors, LED and reflective dental lighting, dental suction units, and steam sterilizers for dental offices.
The company’s products are classified under FDA’s Class I and Class II regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Midmark Corporation is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Midmark Corporation manufacture?
Midmark Corporation specializes in dental and healthcare equipment. Their primary products include stationary intraoral digital dental X-ray systems, electric and examination dental chairs with reusable headrests, intraoral digital imaging sensors, LED and reflective dental lighting, dental suction systems, and steam sterilizers. These devices are designed to support diagnostic and treatment processes in dental offices.
Where is Midmark Corporation based?
Midmark Corporation is headquartered in the United States. While the company operates globally, its primary location and administrative base are within the US.
Which regulatory registries list Midmark Corporation’s devices?
Midmark Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability.
How are Midmark Corporation’s devices classified under FDA regulations?
Midmark Corporation’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on the specific device type and its intended use.
AI-generated from registry data and not verified by a human reviewer.
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 22 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark PREVA IntraOral Dental X-ray System | DCD7DE-W1Y/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | 153910-002 | FDA UDI | Class I | Active |
| Midmark | 9A378001-813 | FDA UDI | Class I | Active |
| Preva, 76" Reach, Gray, 12" Cone | DPD7-G1P | FDA UDI | Class II | Active |
| Midmark | 9A500001-864 | FDA UDI | Class I | Active |
| Midmark | 630-011 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H/SB | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV5-G2A/H/S4 | FDA UDI | Class II | Active |
| Midmark | 1531018-011 | FDA UDI | Class I | Active |
| Midmark | 9A382001-861 | FDA UDI | Class I | Active |
| Midmark | DCD5-G2Z/S2 | FDA UDI | Class II | Active |
| Midmark | 253-007 | FDA UDI | Class I | Active |
| Midmark | M9-041 | FDA UDI | Class II | Active |
| Midmark | P72/G10 | FDA UDI | Class I | Active |
| Midmark | 9A386001-999 | FDA UDI | Class I | Active |
| Midmark | P32SC/CV6R | FDA UDI | Class I | Active |
| Midmark | M11-041 / 9A682001 | FDA UDI | Class II | Active |
| Midmark | DCV6-G2X/H/S2 | FDA UDI | Class II | Active |
| Midmark | 604 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark | DCV8-G2X/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A382001-854 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-G2N | FDA UDI | Class II | Active |
| Midmark | DCD5-G1Z/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD8-G2N/S2 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐W1B/S2 | FDA UDI | N/A | Active |
| Ritter | 255-004 | FDA UDI | Class I | Active |
| Midmark | 9A378001-848 | FDA UDI | Class I | Active |
| Midmark | 9A378001-850 | FDA UDI | Class I | Active |
| Midmark | DCDM-G0Z/H/S2 | FDA UDI | Class II | Active |
| Midmark | DCD7-G2Z/S2 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5-W2Z/H/S2 | FDA UDI | Class II | Active |
| Midmark | 9A384001-999 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7016/H | FDA UDI | Class II | Active |
| Midmark Progeny Imaging Software | 60-A0004 | FDA UDI | Class II | Active |
| Midmark | 9A380001-999 | FDA UDI | Class I | Active |
| Midmark IQvitals® Device with touchscreen - Blood Pressure, Temperature and SpO | 1-100-1615 | FDA UDI | Class II | Active |
| Midmark | 9A739001-846 | FDA UDI | Class I | Active |
| Midmark Intraoral Digital Sensor | XSVP-08 | FDA UDI | Class II | Active |
| Preva, 66" Reach, Deutsch | PE7016-D | FDA UDI | Class II | Active |
| Ritter | 255-006 | FDA UDI | Class I | Active |
| Midmark | 153906-010 | FDA UDI | Class I | Unknown |
| Pan system, export | V5100 | FDA UDI | Class II | Active |
| Midmark | 153901-001 | FDA UDI | Class I | Active |
| Midmark | DCV6-G2A/H/S1 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | 30-A2199 | FDA UDI | Class II | Active |
| Midmark | 153740-003 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD7DE-W1X/H | FDA UDI | Class II | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD6-W2A | FDA UDI | Class II | Active |
| Ritter | 9A51001-847 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
- CEpartner4U NL
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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.
Midmark Corporation has one FDA recall record initiated on March 5, 2003, which is recorded as terminated. The recall was due to a potential failure of the pressure relief valve not opening properly.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 5, 2003 | Z-0704-03 | — | terminated | The pressure relief valve may fail to open properly. |