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Midmark 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
LinkedIn: linkedin.com/company/midmark-corporation/posts
Facebook: facebook.com/MidmarkCorporation
Email: [email protected]
Phone: —
PRRC Contact: Adam Clutter
EUDAMED SRN: US-MF-000002581
FDA FEI Number: 1523530
DUNS Number: —

Catalogue (1527)

Page 2 of 31

Device	Model / Reference	Registries	Class	Status
Midmark	029-4739-02	FDA UDI	Class I	Active
Midmark	153906-018	FDA UDI	Class I	Unknown
Midmark	P52/CV6R	FDA UDI	Class I	Active
Ritter	9A51001-867	FDA UDI	Class I	Active
Midmark	9A739001-813	FDA UDI	Class I	Active
Midmark	P32	FDA UDI	Class I	Active
Midmark	DCV5-G2X/H/S1	FDA UDI	Class II	Active
Midmark	DCV5-G1X/H/S4	FDA UDI	Class II	Active
Midmark	P7017V	FDA UDI	Class II	Active
Midmark	9A410001	FDA UDI	Class I	Active
Midmark	9A81001-853	FDA UDI	Class I	Active
Midmark PREVA IntraOral Dental X-ray System	DCD6DE-W2Y/H/SB	FDA UDI	Class II	Active
Midmark	DCV5-G1X/H	FDA UDI	Class II	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD5‐G2N	FDA UDI	Class II	Active
Ritter	230-004	FDA UDI	Class I	Unknown
Midmark	9A684001-813	FDA UDI	Class I	Active
Midmark	9A382001-857	FDA UDI	Class I	Active
Midmark	DCD7-G1Z	FDA UDI	Class II	Active
Midmark OptiMax Digital Sensor System	XSVS-04	FDA UDI	Class II	Active
Midmark	9A179002-849	FDA UDI	Class I	Active
Midmark	153829-002	FDA UDI	Class I	Unknown
Midmark	9A386001-844	FDA UDI	Class I	Active
Midmark OptiMax Digital Sensor System	XSDQ-04	FDA UDI	Class II	Active
Midmark IQvitals® Device Kit with touchscreen - Blood Pressure and Temperature	4-000-0500	FDA UDI	Class II	Active
Midmark	153818-002	FDA UDI	Class I	Active
Ceph Attachmetnt without sensor	C4000	FDA UDI	Class II	Active
Midmark ClearVision Digital Sensor System with Laptop	XSDN-01/L	FDA UDI	Class II	Active
Midmark	029-7244-07	FDA UDI	Class I	Active
Midmark	9A378001-847	FDA UDI	Class I	Active
Midmark	153829-005	FDA UDI	Class I	Unknown
Midmark	DCV5-G2A/H	FDA UDI	Class II	Active
Midmark	647-002	FDA UDI	Class I	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD6-W1A	FDA UDI	Class II	Active
Midmark	1531018-017	FDA UDI	Class I	Active
Midmark	9A179002-844	FDA UDI	Class I	Active
Midmark	9A394001-858	FDA UDI	Class I	Active
Midmark	DCV5-G1X/H/SB	FDA UDI	Class II	Active
Midmark	153818-004	FDA UDI	Class I	Active
Midmark PREVA IntraOral Dental X-ray System	DCD7-W1B/SB	FDA UDI	Class II	Active
Midmark	9A378001-860	FDA UDI	Class I	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD8-G2N	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	DCD5DE‐W1Y/H/S1	FDA UDI	Class II	Active
Midmark Intraoral Digital Sensor	XSVQ-08	FDA UDI	Class II	Active
Midmark	9A390001-870	FDA UDI	Class I	Active
Midmark	9A394001-845	FDA UDI	Class I	Active
Midmark PREVA IntraOral Dental X-ray System	DCDM-G0N/H/S1	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	DCD7-W2B/SB	FDA UDI	Class II	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD7-W2Z/H	FDA UDI	Class II	Active
Midmark	9A739001-845	FDA UDI	Class I	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD6DE-W2Y/H	FDA UDI	Class II	Active

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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.

Date	Recall No.	Class	Status	Reason
Mar 5, 2003	Z-0704-03	—	terminated	The pressure relief valve may fail to open properly.