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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 19 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark | 153963-000 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone | FDA UDI | Class II | Active |
| Midmark | 9A512001-861 | FDA UDI | Class I | Active |
| Midmark | P52SC/CV6R | FDA UDI | Class I | Active |
| Ritter | 9A51001-854 | FDA UDI | Class I | Active |
| Prep Kit - Midmark IQholter, 5-lead | 2-100-0080 | FDA UDI | Class II | Active |
| Midmark | 153901-004 | FDA UDI | Class I | Active |
| Disposable Spirometer Mouthpieces | 2-100-1205 | FDA UDI | Class II | Active |
| Ritter | 9A337001-856 | FDA UDI | Class I | Active |
| Midmark | DCV7-G2A/H/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | P7017GM | FDA UDI | Class II | Active |
| Ritter | 9A337001-857 | FDA UDI | Class I | Active |
| Midmark | 9A386001-813 | FDA UDI | Class I | Active |
| Midmark | 153915-004 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5‐W1B | FDA UDI | Class II | Active |
| Midmark | 153640-001 | FDA UDI | Class I | Active |
| Midmark | 9A394001-846 | FDA UDI | Class I | Active |
| Midmark | 9A739001-849 | FDA UDI | Class I | Active |
| M9 Ultraclave | M9-020 | FDA UDI | Class II | Active |
| Ritter | M9-042 / 9A599001 | FDA UDI | Class II | Active |
| Midmark | P32/P5 | FDA UDI | Class I | Active |
| Midmark | DCV5-G2A/H/S1 | FDA UDI | Class II | Active |
| Midmark | 9A378001-867 | FDA UDI | Class I | Active |
| Ritter | 203-014 | FDA UDI | Class I | Active |
| Midmark | P22SC/G3 | FDA UDI | Class I | Active |
| Midmark | 250-003 | FDA UDI | Class I | Active |
| Midmark | P14 | FDA UDI | Class I | Active |
| Midmark | IQvitals Zone w/Masimo SPO2 | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | CV10R | FDA UDI | Class I | Active |
| Midmark | 153963-008 | FDA UDI | Class I | Active |
| Ritter | 9A51001-866 | FDA UDI | Class I | Active |
| Midmark Iqholter® Plug-In Software | P/N 4-100-3140 | FDA UDI | Class II | Active |
| Midmark | G6-050 | FDA UDI | Class I | Active |
| Ritter | 9A337001-844 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0B/H/S2 | FDA UDI | Class II | Active |
| Midmark | P72/P10 | FDA UDI | Class I | Active |
| Midmark | P72/CV10R | FDA UDI | Class I | Active |
| Midmark | 153829-006 | FDA UDI | Class I | Unknown |
| Midmark | 1531017-000 | FDA UDI | Class I | Active |
| Midmark | 604 Manual Examination Table | FDA UDI | Class I | Active |
| Midmark | 9A82001-865 | FDA UDI | Class I | Active |
| Midmark | P72SC/G10 | FDA UDI | Class I | Active |
| Midmark | P52SC/CV6 | FDA UDI | Class I | Active |
| Midmark | 647-004 | FDA UDI | Class I | Active |
| Midmark | DCVM-G0X/H/S3 | FDA UDI | Class II | Active |
| Midmark | 641-002 | FDA UDI | Class I | Active |
| Preva, 66" Reach, Gray W/Two Stud Mount, 12" Cone | DPD6-G2P | FDA UDI | Class II | Active |
| Ritter M9 Ultraclave | M9-022R | FDA UDI | Class II | Active |
| Midmark | DCD5-G2Z/SB | 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. |